CasNo.1633-82-5,C3H6Cl2O2S 3-Chloropropanesulfonyl chloride 1633-82-5,(1633-82-5) Suppliers

1 Metric Ton	Negotiable

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Purity: 99.5%
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3-Chloropropanesulfonyl chloride 1633-82-5 C3H6Cl2O2S

Quick Details

Appearance:Powder
Application:1633-82-5
PackAge:Aluminium Foil Bag and Paper Drum
ProductionCapacity:100|Metric Ton|Day
Storage:1MT
Transportation:By Sea/Air/DHL

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Details:

3-Chloropropanesulfonyl chloride Basic information

Product Name:	3-Chloropropanesulfonyl chloride
Synonyms:	3-chloropropylsulfonylchloride;chloro-propanesulfonylchlorid;gamma-chloropropanesulfonylchloride;tl136;3-CHLORO-1-PROPANESULFONYL CHLORIDE;3-CHLOROPROPANESULFONYL CHLORIDE;3-CHLOROPROPANESULPHONYL CHLORIDE;Cpsc3-ChloropropanesulfonylChloride
CAS:	1633-82-5
MF:	C3H6Cl2O2S
MW:	177.05
EINECS:	216-646-3
Product Categories:	Organic Building Blocks;Sulfonyl Halides;Sulfur Compounds;Intermediates;Miscellaneous Reagents;Sulfonyl Chlorides;Building Blocks;Chemical Synthesis;Organic Building Blocks;Sulfonyl Halides;Sulfur Compounds
Mol File:	1633-82-5.mol

3-Chloropropanesulfonyl chloride Chemical Properties

Boiling point	70 °C0.5 mm Hg(lit.)
density	1.456 g/mL at 25 °C(lit.)
refractive index	n20/D 1.489(lit.)
Fp	>230 °F
solubility	Soluble in dichloromethane, ethyl Acetate and hexane.
form	Liquid
color	Clear colorless to light brown
Sensitive	Lachrymatory
BRN	1754119
CAS DataBase Reference	1633-82-5(CAS DataBase Reference)

Safety Information

Hazard Codes	C
Risk Statements	34-36/37
Safety Statements	26-36/37/39-45-24/25
RIDADR	UN 3265 8/PG 2
WGK Germany	3
RTECS	TZ6670000
F	10-19-21
Hazard Note	Corrosive/Lachrymatory
HazardClass	8
PackingGroup	II

MSDS Information

Provider	Language
3-Chloropropanesulfonyl chloride	English
ACROS	English
SigmaAldrich	English
ALFA	English

3-Chloropropanesulfonyl chloride Usage And Synthesis

Chemical Properties	clear colorless to light brown liquid
Uses	Generation and trapping of the derived sulfene with imines and glyoxylates in the presence of chinchona alkaloids provide chiral sultams1 and sultones.2
Uses	Intermediate used in the preparation of many enzymatic inhibitors