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301949

(1R)-(−)-10-Camphorsulfonyl chloride

97%

Synonym(s):

(−)-Camphor-10-sulfonyl chloride, (1R)-Camphor-10-sulfonic acid chloride

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About This Item

Empirical Formula (Hill Notation):
C10H15ClO3S
CAS Number:
39262-22-1
Molecular Weight:
250.74
UNSPSC Code:
12352115
NACRES:
NA.22
PubChem Substance ID:
24858220
MDL number:
MFCD00064155
Beilstein/REAXYS Number:
3205975
Assay:
97%
Form:
solid
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assay

97%

form

solid

optical activity

[α]18/D −33°, c = 3 in chloroform

mp

66-68 °C (lit.)

SMILES string

[H][C@]12CC[C@](CS(Cl)(=O)=O)(C(=O)C1)C2(C)C

InChI

1S/C10H15ClO3S/c1-9(2)7-3-4-10(9,8(12)5-7)6-15(11,13)14/h7H,3-6H2,1-2H3/t7-,10-/m0/s1

InChI key

BGABKEVTHIJBIW-XVKPBYJWSA-N

pictograms

Corrosion
GHS05

signalword

Danger

hcodes

H314

Hazard Classifications

Skin Corr. 1B

Storage Class

8A - Combustible corrosive hazardous materials

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
1323200V
1323200
MKBL2938V
MKBL0408V
MKBJ5663V

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T Jira et al.
Die Pharmazie, 48(11), 829-833 (1993-11-01)
Investigations on direct separation by RP-HPLC of selected enantiomeric beta-adrenergic active agents are described. R- and S-1-phenylethylisocyanate (PEIC) as well as (1S)-(+)-campher-10-sulfonylchloride (CSC) are used for the derivatization of the compounds. Correlations between chromatographic data and various influences (pH, temperature

Global Trade Item Number

SKUGTIN
301949-5G04061833037911