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5-甲氧基吲哚-3-甲醛

5-甲氧基吲哚-3-甲醛用途

1. 用作医药中间体。

2. 用作有机合成中间体。

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5-甲氧基吲哚-3-甲醛名称

[ CAS 号 ]:
10601-19-1

[ 中文名 ]:
5-甲氧基吲哚-3-甲醛

[ 英文名 ]:
5-Methoxy-1H-indole-3-carbaldehyde

[中文别名 ]:

[英文别名 ]:

5-Methoxy-1H-indole-3-carbaldehyde
1H-Indole-3-carboxaldehyde, 5-methoxy-
5-METHOXY-3-INDOLECARBALDEHYDE
5-methoxyindole-3-formaldehyde
3-Formyl-5-methoxyindole
5-Methoxyindole-3-carboxyaldehyde
5-methoxy-1H-indole-3-carboxaIdehyde
5-METHOXYINDOLYL-3-ALDEHYDE
5-methoxyindole-3-carbaldehyde
5-methoxy-1H-indole-3-carboxaldehyde

5-甲氧基吲哚-3-甲醛物理化学性质

[ 密度 ]:
1.3±0.1 g/cm3

[ 沸点 ]:
375.2±22.0 °C at 760 mmHg

[ 熔点 ]:
179-183 °C(lit.)

[ 分子式 ]:
C₁₀H₉NO₂

[ 分子量 ]:
175.184

[ 闪点 ]:
180.7±22.3 °C

[ 精确质量 ]:
175.063324

[ PSA ]:
42.09000

[ LogP ]:
1.60

[ 外观性状 ]:
淡黄色晶体

[ 蒸汽压 ]:
0.0±0.8 mmHg at 25°C

[ 折射率 ]:
1.680

[ 储存条件 ]:
存放于惰性气体之中;避免空气

[ 水溶解性 ]:
insoluble

5-甲氧基吲哚-3-甲醛MSDS

5-甲氧基吲哚-3-甲醛安全信息

[ 符号 ]:

GHS07

[ 信号词 ]:
Warning

[ 危害声明 ]:
H315-H319-H335

[ 警示性声明 ]:
P261-P305 + P351 + P338

[ 危害码 (欧洲) ]:
Xi: Irritant;

[ 风险声明 (欧洲) ]:
R36/37/38

[ 安全声明 (欧洲) ]:
S24/25

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

[ WGK德国 ]:
3

[ 海关编码 ]:
2933990090

5-甲氧基吲哚-3-甲醛合成路线

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5-甲氧基吲哚-3-甲醛上游产品

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5-甲氧基吲哚-3-甲醛海关

[ 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%

5-甲氧基吲哚-3-甲醛文献

Tryptophan 2,3-dioxygenase (TDO) inhibitors. 3-(2-(pyridyl)ethenyl)indoles as potential anticancer immunomodulators.

J. Med. Chem. 54 , 5320, (2011)

Tryptophan catabolism mediated by indoleamine 2,3-dioxygenase (IDO) is an important mechanism of peripheral immune tolerance contributing to tumoral immune resistance. IDO inhibition is thus an active...

Synthesis and antimicrobial activity of cholic acid hydrazone analogues.

Eur. J. Med. Chem. 45 , 2307, (2010)

Synthesis and antimicrobial activity of cholic acid analogues 4a-t are reported. The synthesis of 4a-t was accomplished from ethylcholate 2. The hydrazone moiety was introduced via coupling of the cho...

Synthesis and in vitro characterization of ionone-based chalcones as novel antiandrogens effective against multiple clinically relevant androgen receptor mutants.

Invest. New Drugs 28 , 291, (2010)

A crucial event in prostate cancer progression is the transition from a hormone-sensitive to a lethal castration-refractory disease state. The antagonist-to-agonist conversion due to mutation in AR is...

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