21382
(1R)-(-)-10-樟脑磺酰氯
97.0-103.0% (AT)
别名:
(-)-樟脑-10-磺酰氯, (1R)-樟脑-10-磺酰氯
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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
PubChem Substance ID:
UNSPSC Code:
23151817
Beilstein/REAXYS Number:
3205975
MDL number:
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
grade
derivatization grade ((chiral))
assay
97.0-103.0% (AT)
optical activity
[α]20/D −32±2°, c = 1% in chloroform
storage temp.
2-8°C
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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