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6-溴吲哚

6-溴吲哚用途

6-溴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。

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6-溴吲哚名称

[ CAS 号 ]:
52415-29-9

[ 中文名 ]:
6-溴吲哚

[ 英文名 ]:
6-bromoindole

[中文别名 ]:

6-溴-1H-吲哚

[英文别名 ]:

6-brom-1H-indole
6-BROMINDOL
6-Bromoindole
bromoindole-6
6-Bromo-1H-indole
6-bromo-1 H-indole
MFCD00238550

6-溴吲哚生物活性

[ 描述 ]:

6-溴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]

6个-溴吲哚试剂

6-溴吲哚物理化学性质

[ 密度 ]:
1.7±0.1 g/cm3

[ 沸点 ]:
316.9±15.0 °C at 760 mmHg

[ 熔点 ]:
92-96 °C(lit.)

[ 分子式 ]:
C₈H₆BrN

[ 分子量 ]:
196.04

[ 闪点 ]:
145.5±20.4 °C

[ 精确质量 ]:
194.968353

[ PSA ]:
15.79000

[ LogP ]:
2.91

[ 外观性状 ]:
白色至棕色粉末

[ 蒸汽压 ]:
0.0±0.7 mmHg at 25°C

[ 折射率 ]:
1.712

[ 储存条件 ]:
存放于惰性气体之中;避免光,空气

6-溴吲哚MSDS

6-溴吲哚安全信息

[ 符号 ]:

GHS07

[ 信号词 ]:
Warning

[ 危害声明 ]:
H315-H319-H335

[ 警示性声明 ]:
P261-P305 + P351 + P338

[ 个人防护装备 ]:
dust mask type N95 (US);Eyeshields;Gloves

[ 危害码 (欧洲) ]:
Xi:Irritant

[ 风险声明 (欧洲) ]:
R36/37/38

[ 安全声明 (欧洲) ]:
S26-S36-S37/39

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

[ WGK德国 ]:
3

[ 海关编码 ]:
2942000000

6-溴吲哚合成路线

6-溴吲哚上下游产品

6-溴吲哚上游产品

6-溴吲哚下游产品

6-溴吲哚海关

[ 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-溴吲哚文献

Indoline derivatives as 5-HT(2C) receptor agonists.

Bioorg. Med. Chem. Lett. 14 , 2367-2370, (2004)

A series of 1-(1-indolinyl)-2-propylamines was synthesised and evaluated as 5-HT(2C) receptor agonists for the treatment of obesity. The general methods of synthesis of the precursor indoles are descr...

Synthesis and biological evaluation of achiral indole-substituted titanocene dichloride derivatives.

Int J Med Chem 2012 , 905981, (2015)

Six new titanocene compounds have been isolated and characterised. These compounds were synthesised from their fulvene precursors using Super Hydride (LiBEt3H) followed by transmetallation with titani...

Enantioselective total syntheses of (+)-arborescidine A, (-)-arborescidine B, and (-)-arborescidine C.

J. Org. Chem. 69 , 1283-1289, (2004)

Described are the first enantioselective total syntheses of (+)-arborescidine A ((+)-1), (-)-arborescidine B ((-)-2), and (-)-arborescidine C ((-)-3), via routes that proceeded in five steps and 50% o...

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