5-Chloroindole-2-carboxylic acid


  • CasNo 10517-21-2
  • Purity 99%
Inquery

5-Chloroindole-2-carboxylic acid 10517-21-2 with purity >99% Low price in stock

  • Molecular Formula: C9H6ClNO2
  • Molecular Weight: 195.605
  • Appearance/Colour: light pink to beige or light brown powder 
  • Vapor Pressure: 7.12E-09mmHg at 25°C 
  • Melting Point: 283-287 °C 
  • Refractive Index: 1.5790 (estimate) 
  • Boiling Point: 449.7 °C at 760 mmHg 
  • PKA: 4.26±0.30(Predicted) 
  • Flash Point: 225.8 °C 
  • PSA: 53.09000 
  • Density: 1.548 g/cm3 
  • LogP: 2.51950 

5-Chloroindole-2-carboxylic acid(Cas 10517-21-2) Usage

InChI:InChI=1/C9H6ClNO2/c10-6-1-2-7-5(3-6)4-8(11-7)9(12)13/h1-4,11H,(H,12,13)/p-1

10517-21-2 Relevant articles

Synthesis and Biological Evaluation of Indole-2-carbohydrazide Derivatives as Anticancer Agents with Anti-angiogenic and Antiproliferative Activities

Zhang, Jianqiang,Liu, Tongyang,Chen, Mei,Liu, Feifei,Liu, Xingyuan,Zhang, Jihong,Lin, Jun,Jin, Yi

, p. 1181 - 1192 (2018)

A novel series of indole-2-carbohydrazid...

Preparation method of indole-2-formic acid derivative

-

Paragraph 0046-0048, (2020/07/14)

The invention discloses a preparation me...

Design and synthesis of novel 2,3-dihydropyrazino[1,2-a]indole-1,4-dione derivatives as antiproliferative EGFR and BRAFV600E dual inhibitors

Abdelrahman, Mostafa H.,Abdu-Allah, Hajjaj H. M.,Abou-Ghadir, Ola F.,Al-Wahaibi, Lamya H.,Ali, Asmaa T.,Farghaly, Hatem S.,Gouda, Ahmed M.,Salem, Ola I. A.,Trembleau, Laurent,Youssif, Bahaa G. M.

, (2020/09/15)

Recent studies have shown additive and s...

Synthesis, and evaluation of in vitro and in vivo anticancer activity of 14-substituted oridonin analogs: A novel and potent cell cycle arrest and apoptosis inducer through the p53-MDM2 pathway

Shen, Qing-Kun,Deng, Hao,Wang, Shi-Ben,Tian, Yu-Shun,Quan, Zhen-Shan

, p. 15 - 31 (2019/04/10)

A series of novel oridonin derivatives b...

ANTIBACTERIAL COMPOUNDS

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Page/Page column 86-89, (2019/11/04)

The present application provides compoun...

10517-21-2 Process route

5-chloro-indole-2-carboxylic acid ethyl ester
4792-67-0

5-chloro-indole-2-carboxylic acid ethyl ester

5-chloro-1H-Indole-2-carboxylic acid
10517-21-2

5-chloro-1H-Indole-2-carboxylic acid

Conditions
Conditions Yield
With water; sodium hydroxide; In ethanol; at 40 ℃;
96%
5-chloro-indole-2-carboxylic acid ethyl ester; With sodium hydroxide; In methanol; water; for 1h; Reflux; Green chemistry;
With hydrogenchloride; In methanol; water; at 40 ℃; pH=3 - 4; Green chemistry;
92.5%
5-chloro-indole-2-carboxylic acid ethyl ester; With sodium hydroxide; In ethanol; for 3h; Reflux;
With acetic acid; In ethanol; water; pH=5; Cooling with ice;
90%
With sodium hydroxide; In ethanol; water; at 70 ℃; for 2h;
89%
With potassium hydroxide;
With lithium aluminium tetrahydride; In tetrahydrofuran; at 0 - 20 ℃; for 2h; Inert atmosphere;
With sodium hydroxide; In ethanol; for 3h; Reflux;
With water; Alkaline conditions;
(Z)-4-(2,4-dichloro-benzylidene)-2-phenyloxazole-5(4H)-one

(Z)-4-(2,4-dichloro-benzylidene)-2-phenyloxazole-5(4H)-one

5-chloro-1H-Indole-2-carboxylic acid
10517-21-2

5-chloro-1H-Indole-2-carboxylic acid

Conditions
Conditions Yield
With ethanol; sodium hydrogencarbonate; copper(I) bromide; In N,N-dimethyl-formamide; at 20 - 140 ℃; Reagent/catalyst; Solvent; Temperature;
76%

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    (2S)-[(5-chloro-1H-indole-2-carbonyl)-amino]-3-phenyl-propionic acid methyl ester

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    (2R,3S)-3-[(5-Chloro-1H-indole-2-carbonyl)-amino]-4-cyclohexyl-2-hydroxy-butyric acid isopropyl ester

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