推荐产品
蒸汽压
1 mmHg ( 88 °C)
产品线
ReagentPlus®
方案
≥99.0%
沸点
134 °C/10 mmHg (lit.)
mp
65-69 °C (lit.)
66-69 °C
溶解性
methylene chloride: 0.2 g/mL, clear
benzene-d6: freely soluble(lit.)
chloroform: freely soluble(lit.)
ethanol: freely soluble(lit.)
water: insoluble(lit.)
SMILES字符串
CC1=CC(OP(OC)(OC)=S)=CC=C1SC([2H])([2H])[2H]
Cc1ccc(cc1)S(Cl)(=O)=O
InChI
1S/C7H7ClO2S/c1-6-2-4-7(5-3-6)11(8,9)10/h2-5H,1H3
InChI key
YYROPELSRYBVMQ-UHFFFAOYSA-N
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法律信息
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
警示用语：
Danger
危险分类
Eye Dam. 1 - Met. Corr. 1 - Skin Irrit. 2 - Skin Sens. 1
储存分类代码
8B - Non-combustible corrosive hazardous materials
WGK
WGK 1
闪点(°F)
262.4 °F - closed cup
闪点(°C)
128 °C - closed cup
个人防护装备
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
法规信息
新产品
p-Toluenesulfonyl Chloride.
Whitaker DT, et al.
e-EROS Encyclopedia of Reagents for Organic Synthesis. (2006)
Balázs Pásztói et al.
Polymers, 12(11) (2020-11-01)
Endfunctional polymers possess significant industrial and scientific importance. Sulfonyl endgroups, such as tosyl and nosyl endfunctionalities, due their ease of substitution are highly desired for a variety of polymer structures. The sulfonylation of hydroxyl-terminated polyisobutylene (PIB-OH), a chemically and thermally
[Degradation reactions of oral antidiabetics. 2. Reaction of arylsulfonylureas with 4-toluenesulfonyl chloride].
H Egg et al.
Archiv der Pharmazie, 320(3), 253-257 (1987-03-01)
I M Kung et al.
Biomaterials, 16(8), 649-655 (1995-05-01)
Three different surface modifications were conducted on the membranes of double-layer alginate/poly(L-lysine) microcapsules with tosyl chloride-activated poly(ethylene glycol), cyanuric chloride-activated poly(ethylene glycol) and tosyl chloride-activated poly(vinyl alcohol), separately. All these surface modifications strengthen the microcapsular membranes. Of the three surface-modified
Simple, Mild, and Practical esterification, Thioesterification, and amide formation utilizing p-toluenesulfonyl chloride and N-Methylimidazole.
Wakasugi K, et al.
Advanced Synthesis & Catalysis, 345(11), 1209-1214 (2003)
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