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关于此项目
经验公式(希尔记法):
C10H15ClO3S
化学文摘社编号:
分子量:
250.74
UNSPSC Code:
12352115
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
3205975
产品名称
(1R)-(-)-10-樟脑磺酰氯, 97%
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
SMILES string
[H][C@]12CC[C@](CS(Cl)(=O)=O)(C(=O)C1)C2(C)C
InChI key
BGABKEVTHIJBIW-XVKPBYJWSA-N
assay
97%
form
solid
optical activity
[α]18/D −33°, c = 3 in chloroform
mp
66-68 °C (lit.)
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signalword
Danger
hcodes
Hazard Classifications
Skin Corr. 1B
存储类别
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
法规信息
新产品
此项目有
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
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