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Merck
CN

29550

Sigma-Aldrich

环己基氨基磺酸

≥98.0% (T)

别名:

环己氨磺酸, 环拉酸

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About This Item

经验公式(希尔记法):
C6H13NO3S
CAS号:
分子量:
179.24
Beilstein:
2208885
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

质量水平

检测方案

≥98.0% (T)

形式

solid

mp

~180 °C (dec.)

溶解性

dioxane: 1 g/10 mL, clear, colorless (hot)

SMILES字符串

OS(=O)(=O)NC1CCCCC1

InChI

1S/C6H13NO3S/c8-11(9,10)7-6-4-2-1-3-5-6/h6-7H,1-5H2,(H,8,9,10)

InChI key

HCAJEUSONLESMK-UHFFFAOYSA-N

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一般描述

The N-cyclohexylsulfamic acid salts of well−known therapeutic agents were prepared.

WGK

WGK 2

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, type N95 (US)


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Modification of physical properties of certain antitussive and antihistaminic agents by formation of N-cyclohexylsulfamate salts.
J A CAMPBELL et al.
Journal of pharmaceutical sciences, 51, 931-934 (1962-10-01)
Lin Yi et al.
Analytical and bioanalytical chemistry, 386(3), 666-674 (2006-05-26)
Characterizing the biological effects of metabolic transformations (or biotransformation) is one of the key steps in developing safe and effective pharmaceuticals. Sulfate conjugation, one of the major phase II biotransformations, is the focus of this study. While this biotransformation typically

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