3-Chloro-1-propanesulfonyl chloride

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Names

[ CAS No. ]:
1633-82-5

[ Name ]:
3-Chloro-1-propanesulfonyl chloride

[Synonym ]:
1-Propanesulfonyl chloride, 3-chloro-
EINECS 216-646-3
3-Chloro-1-propanesulfonyl chloride
γ-Chloropropanesulfonyl chloride
MFCD00007463
3-Chloropropane-1-sulfonyl chloride

Chemical & Physical Properties

[ Density]:
1.5±0.1 g/cm3

[ Boiling Point ]:
262.1±0.0 °C at 760 mmHg

[ Molecular Formula ]:
C3H6Cl2O2S

[ Molecular Weight ]:
177.049

[ Flash Point ]:
92.3±22.6 °C

[ Exact Mass ]:
175.946548

[ PSA ]:
42.52000

[ LogP ]:
1.22

[ Vapour Pressure ]:
0.0±0.5 mmHg at 25°C

[ Index of Refraction ]:
1.477

MSDS

Toxicological Information

CHEMICAL IDENTIFICATION

RTECS NUMBER :
TZ6670000
CHEMICAL NAME :
Propanesulfonyl chloride, chloro-
CAS REGISTRY NUMBER :
1633-82-5
BEILSTEIN REFERENCE NO. :
1754119
LAST UPDATED :
199612
DATA ITEMS CITED :
1
MOLECULAR FORMULA :
C3-H6-Cl2-O2-S
MOLECULAR WEIGHT :
177.05
WISWESSER LINE NOTATION :
WSG3 YG

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :
LCLo - Lowest published lethal concentration
ROUTE OF EXPOSURE :
Inhalation
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
1160 mg/m3/10M
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
NDRC** National Defense Research Committee, Office of Scientific Research and Development, Progress Report. Volume(issue)/page/year: NDCrc-132,AUG1942

Safety Information

[ Symbol ]:

GHS05, GHS07

[ Signal Word ]:
Danger

[ Hazard Statements ]:
H314-H335

[ Precautionary Statements ]:
P261-P280-P305 + P351 + P338-P310

[ Personal Protective Equipment ]:
Faceshields;full-face respirator (US);Gloves;Goggles;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter

[ Hazard Codes ]:
C:Corrosive;

[ Risk Phrases ]:
R34;R36/37

[ Safety Phrases ]:
S26-S36/37/39-S45-S24/25

[ RIDADR ]:
UN 3265 8/PG 2

[ WGK Germany ]:
3

[ RTECS ]:
TZ6670000

[ Packaging Group ]:
II

[ Hazard Class ]:
8

[ HS Code ]:
2904909090

Precursor & DownStream

Precursor

  • 3-Chloropropylamine hydrochloride
  • 1,3-Propanesultone
  • oxathiolane 2-oxide
  • 3-MERCAPTO-1-PROPANOL
  • Thietane
  • 1-Chloropropane
  • Sodium 3-hydroxypropane-1-sulphonate
  • 1-Propanesulfonyl chloride
  • Chlorine
  • acetic acid

DownStream

  • 4-(3-chloropropylsulfonyl)morpholine
  • 1-(3-chloropropylsulfonyl)-4-methylpiperazine
  • 1-propanesulfonamide, 3-chloro-N,N-dimethyl-
  • N-(tert-butyl)-3-chloropropane-1-sulfonamide
  • 1-(CYCLOPROPYLSULFONYL)PIPERIDINE-4-CARBOXAMIDE
  • 3-氯丙烷-1-磺酰胺
  • 2-(3-Bromophenyl)isothiazolidine 1,1-dioxide
  • 2-(2-pyridin-4-ylethyl)-1,2-thiazolidine 1,1-dioxide
  • 3-Chloro-1-propanesulfonic acid
  • 1-(3-chloropropylsulfonyl)-3-(3,5-dichlorophenyl)imidazolidine-2,4-dione

Customs

[ HS Code ]: 2904909090

[ Summary ]:
HS:2904909090 sulphonated, nitrated or nitrosated derivatives of hydrocarbons, whether or not halogenated VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:5.5% General tariff:30.0%

Articles

Catalytic asymmetric formation of beta-sultams.

Org. Lett. 9 , 2007, (2007)

beta-Sultams, highly strained sulfonyl analogues of beta-lactams, were prepared enantio- and diastereoselectively by tertiary amine catalyzed [2 + 2] cycloaddition reactions. The title compounds are p...

Catalytic enantio- and diastereoselective formation of beta-sultones: ring-strained precursors for enantioenriched beta-hydroxysulfonyl derivatives.

Angew. Chem. Int. Ed. Engl. 46 , 2685, (2007)

Functionalized chiral ionic liquid as recyclable organocatalyst for asymmetric Michael addition to nitrostyrenes. Ni B, et al.

Green Chem. 9(7) , 737-739, (2007)


More Articles


Related Compounds

  • 3-Methoxy-1-propanesulfonyl chloride
  • 3-Chloro-1-benzothiophene-2-carbonyl chloride
  • 3-chloro-1,2-benzodithiol-1-ium,chloride
  • 3-chloro-1-(dodecylsulfanylmethyl)pyridin-1-ium,chloride
  • 3-chloro-1-(octylsulfanylmethyl)pyridin-1-ium,chloride
  • 3-chloro-1,2-thiazole-4-sulfonyl chloride
  • 1-(4-chloro-2-methylphenyl)-4-(4-methylpiperidin-1-yl)-1H-pyrazolo[3,4-d]pyrimidine
  • N-benzyl-1-(4-chloro-2-methylphenyl)-N-ethyl-1H-pyrazolo[3,4-d]pyrimidin-4-amine
  • 1-(5-chloro-2-methylphenyl)-N-(2-methoxybenzyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine
  • Adamantanyl[1-(5-chloro-2-methylphenyl)pyrazolo[4,5-e]pyrimidin-4-yl]amine
  • 1-(5-chloro-2-methylphenyl)-N-(3,4-dimethoxyphenethyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine
  • N-benzyl-1-(5-chloro-2-methylphenyl)-N-methyl-1H-pyrazolo[3,4-d]pyrimidin-4-amine
  • 1-(5-chloro-2-methylphenyl)-N-(2,4-dimethylphenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine
  • N-(1,3-benzodioxol-5-yl)-1-(5-chloro-2-methylphenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine
  • 1-(5-chloro-2-methylphenyl)-N-(4-methylphenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine
  • kaempferol 3-O-[alpha-L-rhamnopyranosyl(1->2)-beta-D-glucopyranosyl]-7-O-alpha-L-rhamnopyranoside
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