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对甲苯磺酰肼

对甲苯磺酰肼结构式
对甲苯磺酰肼结构式
品牌特惠专场
常用名 对甲苯磺酰肼 英文名 4-Methylbenzenesulfonhydrazide
CAS号 1576-35-8 分子量 186.232
密度 1.3±0.1 g/cm3 沸点 340.5±35.0 °C at 760 mmHg
分子式 C7H10N2O2S 熔点 103-108 °C(lit.)
MSDS 中文版 美版 闪点 159.7±25.9 °C
符号 GHS02 GHS06
GHS02, GHS06
信号词 Danger

Protecting group free glycosidations using p-toluenesulfonohydrazide donors.

Org. Lett. 10(16) , 3461-3, (2008)

N'-Glycopyranosylsulfonohydrazides are introduced as glycosyl donors for protecting group free synthesis of O-glycosides, glycosyl azides, and oxazolines. Mono- and disaccharides containing a reducing terminal N-acetylglucosamine residue were condensed with p...

Synthesis of some p-toluenesulfonyl-hydrazinothiazoles and hydrazino-bis-thiazoles and their anticancer activity.

Eur. J. Med. Chem. 45(11) , 5080-5, (2010)

A series of novel p-toluenesulfonyl-hydrazinothiazoles and hydrazino-bis-thiazoles derivatives (2a-f, 3a-f and 5-8) were synthesized by initial condensation of p-toluenesulfonylthiosemicarbazide 1 with a series of α-halogenocarbonyls in acetone or dimethylfor...

Vasoconstrictor-induced changes in renal blood flow: role of prostaglandins and histamine.

Am. J. Physiol. 254(4 Pt 2) , F470-6, (1988)

The role of histamine (H) and prostaglandins (PGs) in the renal vasoconstriction prompted by a 10-min intrarenal infusion of norepinephrine (NE, 0.2 micrograms), antidiuretic hormone (ADH, 10 mU), or angiotensin II (ANG II, 0.05 micrograms) was evaluated in a...

Mutagenic activity of p-toluenesulfonhydrazide.

Toxicol. Ind. Health 8(6) , 369-76, (1992)

Toluenesulfonhydrazide (TSH) is a high volume production chemical for which there is relatively little toxicological data. In this study, the mutagenic activity of TSH was determined in the Salmonella/mammalian microsome assay and the in vitro chromosomal abe...

Enantioselective synthesis of trifluoromethyl-substituted cyclopropanes.

Org. Lett. 9 , 2625, (2007)

The reaction of 1-aryl-2,2,2-trifluorodiazoethanes with alkenes, catalyzed by the adamantylglycine-derived dirhodium complex Rh2(R-PTAD)4, generates trifluoromethyl-substituted cyclopropanes with high diastereoselectivity (>94%) and enantioselectivity (88->98...

Dipyrazolo[1,5-a:4',3'-c]pyridines - a new heterocyclic system accessed via multicomponent reaction.

Beilstein J. Org. Chem. 8 , 2223-9, (2012)

The synthesis of dipyrazolo[1,5-a:4',3'-c]pyridines is described. Easily obtainable 5-alkynylpyrazole-4-carbaldehydes, p-toluenesulfonyl hydrazide, and an aldehyde or ketone containing an α-hydrogen atom were reacted in a silver triflate catalyzed multicompon...

Synthesis, characterization and antimicrobial activity of new 1,2,3-selenadiazoles.

Molecules 13(11) , 2740-9, (2008)

The commercially available aromatic polyketones 1a-d were utilized for the synthesis of the multi-arm1,2,3-selenadiazole derivatives 3a-d. The preparation starts with the reaction between compounds 1a-d and p-toluenesulfonyl hydrazide to give the correspondin...

Inhibitors of bacterial cystathionine beta-lyase: leads for new antimicrobial agents and probes of enzyme structure and function.

J. Med. Chem. 50 , 755-64, (2007)

The biosynthesis of methionine is an attractive antibiotic target given its importance in protein and DNA metabolism and its absence in mammals. We have performed a high-throughput screen of the methionine biosynthesis enzyme cystathionine beta-lyase (CBL) ag...

J. Am. Chem. Soc. 115 , 2473, (1993)

J. Am. Chem. Soc. 114 , 966, (1992)