Category: 6972-05-0

Trchunyan, A. A. published the artcileN,N’-dicyclohexylcarbodiimide-sensitive and potassium-dependent proton secretion from anaerobically grown E. coli, Recommanded Product: 1,1-Dimethylthiourea, the publication is Biofizika (1989), 34(2), 322-3, database is CAplus.

Dependence of N,N‘-dicyclohexylcarbodiimide (DCC)-sensitive H⁺ secretion on K⁺ activity was observed This dependence took place only in anaerobically grown Escherichia?coli and only at the structurally intact DCC-sensitive H⁺-ATPase complex and K⁺-ionophore Trk.

Biofizika published new progress about 6972-05-0. 6972-05-0 belongs to catalysis-chemistry, auxiliary class Thiourea,Amine,Aliphatic hydrocarbon chain,Amide, name is 1,1-Dimethylthiourea, and the molecular formula is C13H9FO2, Recommanded Product: 1,1-Dimethylthiourea.

Referemce:
https://courses.lumenlearning.com/boundless-chemistry/chapter/catalysis/,
Catalysis – Wikipedia

Zhou, Ming published the artcileDesign, synthesis and biological evaluation of indeno[1,2-d]thiazole derivatives as potent histone deacetylase inhibitors, Product Details of C3H8N2S, the publication is Bioorganic & Medicinal Chemistry Letters (2013), 23(11), 3200-3203, database is CAplus and MEDLINE.

Novel indeno[1,2-d]thiazole hydroxamic acids were designed, synthesized, and evaluated for histone deacetylases (HDACs) inhibition and antiproliferative activities on tumor cell lines. Most of the tested compounds exhibited HDAC inhibition and antiproliferative activity against both MCF7 and HCT116 cells with GI₅₀ values in the sub-micromolar range. Among them, compound I showed good inhibitory activity against pan-HDAC with IC₅₀ value of 0.14 ¦ÌM and significant growth inhibition on MCF7 and HCT116 cells with GI₅₀ values of 0.869 and 0.535 ¦ÌM, resp.

Bioorganic & Medicinal Chemistry Letters published new progress about 6972-05-0. 6972-05-0 belongs to catalysis-chemistry, auxiliary class Thiourea,Amine,Aliphatic hydrocarbon chain,Amide, name is 1,1-Dimethylthiourea, and the molecular formula is C12H9N3O4, Product Details of C3H8N2S.

Referemce:
https://courses.lumenlearning.com/boundless-chemistry/chapter/catalysis/,
Catalysis – Wikipedia

Takahashi, Hitoe published the artcileSelenoureas and thioureas are effective superoxide radical scavengers in vitro, Product Details of C3H8N2S, the publication is Life Sciences (2005), 76(19), 2185-2192, database is CAplus and MEDLINE.

The authors investigated scavenging of superoxide radicals by selenoureas and thioureas using a highly sensitive and quant. chemiluminescence method. At 330 nM, five selenoureas and five thioureas scavenged fractions of superoxide radicals (O^–₂) ranging from 8.4% to 87.6%. Among five N,N-unsubstituted selenoureas and N,N-unsubstituted thioureas, 1-selenocarbamoylpiperidine and 1-thiocarbamoylpyrrolidine were the most effective scavengers. The study showed that selenoureas could be used as new superoxide anion-scavenging substances.

Life Sciences published new progress about 6972-05-0. 6972-05-0 belongs to catalysis-chemistry, auxiliary class Thiourea,Amine,Aliphatic hydrocarbon chain,Amide, name is 1,1-Dimethylthiourea, and the molecular formula is C8H6ClF3, Product Details of C3H8N2S.

Referemce:
https://courses.lumenlearning.com/boundless-chemistry/chapter/catalysis/,
Catalysis – Wikipedia

Burger, Klaus published the artcileA surprising access route to ¦Á-hetero-substituted methylphosphonate esters, SDS of cas: 6972-05-0, the publication is Chemiker-Zeitung (1988), 112(3), 108-9, database is CAplus.

A mixture of 2,2-bis(trifluoromethyl)oxazolone I and P(OMe)₃ reacts with thiourea, as well as with N,N-dimethylthiourea, morpholinothioamide, and thioacetamide to give 65% (MeO)₂P(O)CH(SMe)NHCH(CF₃)₂.

Chemiker-Zeitung published new progress about 6972-05-0. 6972-05-0 belongs to catalysis-chemistry, auxiliary class Thiourea,Amine,Aliphatic hydrocarbon chain,Amide, name is 1,1-Dimethylthiourea, and the molecular formula is C3H8N2S, SDS of cas: 6972-05-0.

Referemce:
https://courses.lumenlearning.com/boundless-chemistry/chapter/catalysis/,
Catalysis – Wikipedia

Grosso, John A. published the artcileSynthesis of 2-(alkylamino)-5,6- and -6,7-dihydroxy-3,4-dihydroquinazolines and evaluation as potential dopamine agonists, Application In Synthesis of 6972-05-0, the publication is Journal of Medicinal Chemistry (1982), 25(6), 703-8, database is CAplus and MEDLINE.

Based upon the known dopaminergic properties of 2-aminodihydroxy-1,2,3,4-tetrahydronaphthalenes, heterocyclic congeners were prepared Several 2-(alkylamino)-5,6-dihydroxy-3,4-dihydroquinazolines were synthesized and tested for a dopamine-like vasodilatory action in the canine renal artery. The 6,7-disubstituted series had a weak antagonist effect against dopamine. Neither 5,6- nor 6,7-dihydroxy substitution gave dopamine agonists. Measured pK_a values confirmed the expectation that the dihydroquinazolines were more basic than dopamine, one possible reason for the lack of dopamine-like action.

Journal of Medicinal Chemistry published new progress about 6972-05-0. 6972-05-0 belongs to catalysis-chemistry, auxiliary class Thiourea,Amine,Aliphatic hydrocarbon chain,Amide, name is 1,1-Dimethylthiourea, and the molecular formula is C3H8N2S, Application In Synthesis of 6972-05-0.

Referemce:
https://courses.lumenlearning.com/boundless-chemistry/chapter/catalysis/,
Catalysis – Wikipedia

Goerdeler, Joachim published the artcileThioacyl isocyanates. XII. Preparation and comparison of aliphatic, aromatic and heteroaromatic compounds, Related Products of catalysis-chemistry, the publication is Chemische Berichte (1981), 114(2), 549-63, database is CAplus.

Dithiazolones I (R = Me, halomethyl, optionally substituted Ph, CH₂Ph, CO₂Et, CMe₃, CH:CHPh, NMe₂, pyridyl, 2-furyl, 5-methyl-3-isoxazolyl, 5-oxo-1,2,4-dithiazol-3-yl) were prepared by treating RCSNH₂ with ClCOSCl. II were similarly obtained from RCSNH₂ and ClCOCOCl. I and II eliminated S and CO resp. to give S:CRNCO. The latter compounds underwent cycloaddition reaction with imines, norbornene, and morpholinocyclohexene, as well as dimerization. S:CRNCO in which R is a strongly electron-attracting group are less reactive than others.

Chemische Berichte published new progress about 6972-05-0. 6972-05-0 belongs to catalysis-chemistry, auxiliary class Thiourea,Amine,Aliphatic hydrocarbon chain,Amide, name is 1,1-Dimethylthiourea, and the molecular formula is C3H8N2S, Related Products of catalysis-chemistry.

Referemce:
https://courses.lumenlearning.com/boundless-chemistry/chapter/catalysis/,
Catalysis – Wikipedia

Shibuya, Isao published the artcileThe synthesis of heteroaromatic cations containing sulfur or selenium atoms, Computed Properties of 6972-05-0, the publication is Bulletin of the Chemical Society of Japan (1987), 60(7), 2686-8, database is CAplus.

Oxidative cyclocondensation of Me₂NCCl:X⁺CClNMe₂ Cl^– (I; X = N, CH) with NaSH or NaSeH gave 43-95% heteroaromatic cations II (X = N, CH; X¹ = S, Se). Cyclocondensation of I with RCX¹NH₂ (R = Me₂N, Ph, pyrrolidino; X¹ = S, Se) gave 44-73% 6-membered heteroaromatic cations III.

Bulletin of the Chemical Society of Japan published new progress about 6972-05-0. 6972-05-0 belongs to catalysis-chemistry, auxiliary class Thiourea,Amine,Aliphatic hydrocarbon chain,Amide, name is 1,1-Dimethylthiourea, and the molecular formula is C19H17N2NaO4S, Computed Properties of 6972-05-0.

Referemce:
https://courses.lumenlearning.com/boundless-chemistry/chapter/catalysis/,
Catalysis – Wikipedia

Utinans, M. published the artcileSynthesis and properties of 5-(5-amino-3,6-dichloro-1,4-benzoquinon-2-yl)-2-(dimethylamino)thiazoles, COA of Formula: C3H8N2S, the publication is Khimiya Geterotsiklicheskikh Soedinenii (1991), 410-15, database is CAplus.

The reaction of (trichlorobenzoquinonyl)triazole I (R = Cl) with secondary amines gave the corresponding 5-amino derivatives I [R = dialkylamino (II)]. The reduction and redox potentials of some II were studied.

Khimiya Geterotsiklicheskikh Soedinenii published new progress about 6972-05-0. 6972-05-0 belongs to catalysis-chemistry, auxiliary class Thiourea,Amine,Aliphatic hydrocarbon chain,Amide, name is 1,1-Dimethylthiourea, and the molecular formula is C28H41N2P, COA of Formula: C3H8N2S.

Referemce:
https://courses.lumenlearning.com/boundless-chemistry/chapter/catalysis/,
Catalysis – Wikipedia

Lopez, S. published the artcileSpray pyrolysis deposition of Sn₂S₃ thin films, Name: 1,1-Dimethylthiourea, the publication is Semiconductor Science and Technology (1996), 11(3), 433-6, database is CAplus.

Ternary compound Sn^IISn^IVS₃ thin films were prepared on Pyrex glass substrates by the spray pyrolysis process using Sn chloride (SnCl₂) and n,n-dimethylthiourea as starting materials. The depositions were carried out at a substrate temperature of 320¡ã. The identification of the Sn₂S₃ phase was achieved by x-ray diffraction measurements. The optical reflectance and transmittance of the prepared films were used to obtain the variation of the refractive index and the extinction coefficient as a function of the wavelength. These calculated values were used to find the absorption coefficient and the optical bandgap and gave E_g = 1.16 eV. From measurements of the conductance as a function of T^-1, a dark activation energy was determined with a value of 1.02 eV.

Semiconductor Science and Technology published new progress about 6972-05-0. 6972-05-0 belongs to catalysis-chemistry, auxiliary class Thiourea,Amine,Aliphatic hydrocarbon chain,Amide, name is 1,1-Dimethylthiourea, and the molecular formula is C3H8N2S, Name: 1,1-Dimethylthiourea.

Referemce:
https://courses.lumenlearning.com/boundless-chemistry/chapter/catalysis/,
Catalysis – Wikipedia

Burger, Klaus published the artcileHexafluoroacetone as protective group and activating reagent in amino acid and peptide chemistry. 10. Synthesis of 3-(thiazol-4-yl)alanine and 3-(selenazol-4-yl)alanine derivatives from aspartic acid, Computed Properties of 6972-05-0, the publication is Synthesis (1992), 1145-50, database is CAplus.

3-(Thiazol-4-yl)alanines I (R = Ph, 4-MeC₆H₄, 4-MeOC₆H₄, 2-furyl, NMe₂, 4-FC₆H₄, 2-thienyl, H, Me; R¹ = H, Me) and the 3-(selenazol-4-yl)alanine II were obtained from aspartic acid via 2,2-bis(trifluoromethyl)-4-(3-bromo-2-oxopropyl)-1,3-oxazolidin-5-one in a Hantzsch synthesis, using hexafluoroacetone as protective group.

Synthesis published new progress about 6972-05-0. 6972-05-0 belongs to catalysis-chemistry, auxiliary class Thiourea,Amine,Aliphatic hydrocarbon chain,Amide, name is 1,1-Dimethylthiourea, and the molecular formula is C3H8N2S, Computed Properties of 6972-05-0.

Referemce:
https://courses.lumenlearning.com/boundless-chemistry/chapter/catalysis/,
Catalysis – Wikipedia