产品说明
一般描述
5-Chloroindole is a 5-substituted indole. It undergoes electropolymerization to form a redox-active film consisting of a cyclic trimer and chains of linked cyclic trimer (polymer). It is a potential positive allosteric modulator (PAM) of the 5-HT3 receptor. It has been reported as strong inhibitor of the copper dissolution in acidic sodium chloride solution. It has been tested as corrosion inhibitor of mild steel in 1N deaerated sulphuric acid. Synthesis of 5-chloroindole, via nitration of indoline has been described.
5-Chloroindole can be synthesized by using 3-chlorobenzaldehyde as starting reagent.
应用
5-Chloroindole has been used in the synthesis of 5-chloro-3-indole-N,N- dimethylglyoxalamide and 5-chloro-N,N-dimethyltryptamine. It may be used in the synthesis of dyestuffs in the presence of biocatalysts (Escherichia coli expressing multicomponent phenol hydroxylase (mPH) isolated from Pseudomonas sp. strains KL33 and KL28).
5-Chloroindole has been used to study the biotransformation of substituted indoles to indican derivatives in the tissue cultures of Polygonum tinctorium. It may be employed as a monomer in the preparation of redox-active film made up of a cyclic trimer and chains of linked cyclic trimer (polymer).
包装
1, 5 g in glass bottle
基本信息
| 经验(实验)分子式 | C8H6ClN |
| 分子量 | 151.59 |
| Beilstein | 2651 |
| EC 号 | 241-448-9 |
| MDL编号 | MFCD00005672 |
| PubChem化学物质编号 | 24892721 |
| NACRES | NA.22 |
产品性质
| 质量水平 | 100 |
| 测定 | 98% |
| mp | 69-71 ℃ (lit.) |
| SMILES string | Clc1ccc2[nH]ccc2c1 |
| InChI | 1S/C8H6ClN/c9-7-1-2-8-6(5-7)3-4-10-8/h1-5,10H |
| InChI key | MYTGFBZJLDLWQG-UHFFFAOYSA-N |
安全信息
| 储存分类代码 | 13 - Non Combustible Solids |
| WGK | WGK 3 |
| 闪点(F) | Not applicable |
| 闪点(C) | Not applicable |
| 个人防护装备 | Eyeshields, Gloves, type N95 (US) |
