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6-氯吲哚

6-氯吲哚用途

6-氯吲哚是一种生物化学试剂,可作为生物材料或有机化合物用于生命科学相关研究。

6-氯吲哚名称

[ CAS 号 ]:
17422-33-2

[ 中文名 ]:
6-氯吲哚

[ 英文名 ]:
6-Chloro-1H-indole

[中文别名 ]:

6-氯吲哚林

[英文别名 ]:

6-chloro indole
1H-Indole, 6-chloro-
MFCD00005681
6-Chloroindole
6-Cl-indole
EINECS 241-449-4
1H-Indole,6-chloro
6-chlorolindole
6-Chloro-1H-indole

6-氯吲哚生物活性

[ 描述 ]:

6-氯吲哚是一种生物化学试剂,可作为生物材料或有机化合物用于生命科学相关研究。

[ 相关类别 ]:

研究领域 >> 其他

[体外研究]

产品规格6个-氯吲哚；6个-氯-1小时-吲哚；

6-氯吲哚物理化学性质

[ 密度 ]:
1.3±0.1 g/cm3

[ 沸点 ]:
293.0±13.0 °C at 760 mmHg

[ 熔点 ]:
87-90 °C(lit.)

[ 分子式 ]:
C₈H₆ClN

[ 分子量 ]:
151.59

[ 闪点 ]:
158.9±5.4 °C

[ 精确质量 ]:
151.018875

[ PSA ]:
15.79000

[ LogP ]:
2.74

[ 外观性状 ]:
白色结晶粉末

[ 蒸汽压 ]:
0.0±0.6 mmHg at 25°C

[ 折射率 ]:
1.688

[ 储存条件 ]:
存放于惰性气体之中;避免光,空气

[ 稳定性 ]:
Store in Refrigerator

[ 水溶解性 ]:
slightly soluble

6-氯吲哚MSDS

6-氯吲哚安全信息

[ 个人防护装备 ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ 危害码 (欧洲) ]:
Xi:Irritant

[ 风险声明 (欧洲) ]:
R36/37/38

[ 安全声明 (欧洲) ]:
S22-S24/25-S37/39-S26

[ 危险品运输编码 ]:
NONH for all modes of transport

[ WGK德国 ]:
3

[ 海关编码 ]:
2933990090

6-氯吲哚合成路线

6-氯吲哚上下游产品

6-氯吲哚上游产品

6-氯吲哚下游产品

6-氯吲哚海关

[ 海关编码 ]: 2933990090

[ 中文概述 ]:
2933990090. 其他仅含氮杂原子的杂环化合物. 增值税率:17.0%. 退税率:13.0%. 监管条件:无. 最惠国关税:6.5%. 普通关税:20.0%

[ 申报要素 ]: 品名, 成分含量, 用途, 乌洛托品请注明外观, 6－己内酰胺请注明外观, 签约日期

[ Summary ]:
2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

6-氯吲哚文献

Design, synthesis and structure-activity relationship studies of novel and diverse cyclooxygenase-2 inhibitors as anti-inflammatory drugs.

J. Enzyme Inhib. Med. Chem. 29(6) , 846-67, (2014)

Because of the pivotal role of cyclooxygenase (COX) in the inflammatory processes, non-steroidal anti-inflammatory drugs (NSAIDs) that suppress COX activities have been used clinically for the treatme...

Toward prediction of alkane/water partition coefficients.

J. Med. Chem. 51 , 3720-30, (2008)

Partition coefficients were measured for 47 compounds in the hexadecane/water ( P hxd) and 1-octanol/water ( P oct) systems. Some types of hydrogen bond acceptor presented by these compounds to the pa...

Production of substituted L-tryptophans by fermentation.

Appl. Microbiol. 21(5) , 841-3, (1971)

Claviceps purpurea has been shown to produce extracellular l-tryptophan from indole in stirred fermentors. The substrate specificity of this conversion was investigated by using substituted indoles, a...

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