추천 제품
분석
97%
refractive index
n20/D 1.5490 (lit.)
bp
252-253 °C (lit.)
density
1.314 g/mL at 25 °C (lit.)
SMILES string
Cc1cccc(c1)S(Cl)(=O)=O
InChI
1S/C7H7ClO2S/c1-6-3-2-4-7(5-6)11(8,9)10/h2-5H,1H3
InChI key
KFPMLWUKHQMEBU-UHFFFAOYSA-N
일반 설명
m-Toluenesulfonyl chloride can be synthesized via chlorination of m-thiocresol in glacial acetic acid.
애플리케이션
m-Toluenesulfonyl chloride may be used in the synthesis of mesityl-m-tolyl sulfone via reaction with mesitylene.
Reactant involved in they synthesis of biologically active molecules including:
- Small molecule ligands for the Stat3 SH2 domain
- Isoindoline-5-propenehydroxamates for use as histone deactylase inhibitors
- Phenyl-pyrazolylamine-based derivatives as FLT3 kinase inhibitors
- Aryldisulfonamides with antibacterial activity
- Quinazoline analogs for the treatment of Gaucher disease
- 17β-HSD2 inhibitors for the treatment of osteoporosis
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Skin Corr. 1B
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 3
Flash Point (°F)
225.0 °F - closed cup
Flash Point (°C)
107.2 °C - closed cup
개인 보호 장비
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
이미 열람한 고객
Rearrangements of sulfones to sulfinic acids via carbanion intermediates.
Truce WE and Brand WW
The Journal of Organic Chemistry, 35(6), 1828-1833 (1970)
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