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860024-94-8

1H-Indole-1-carboxylic acid, 5-(2-chloroethyl)-2,3-dihydro-, 1,1-diMethylethyl ester

CAS: 860024-94-8

Molecular Formula: C15H20ClNO2

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860024-94-8 - Names and Identifiers

Name 1H-Indole-1-carboxylic acid, 5-(2-chloroethyl)-2,3-dihydro-, 1,1-diMethylethyl ester
Synonyms 5-(2-Chloroethyl)indoline, N-BOC protected
tert-Butyl 5-(2-chloroethyl)indoline-1-carboxylate
tert-Butyl 5-(2-chloroethyl)-2,3-dihydro-1H-indole-1-carboxylate
1H-Indole-1-carboxylic acid, 5-(2-chloroethyl)-2,3-dihydro-, 1,1-diMethylethyl ester
5-(2-Chloroethyl)-2,3-dihydro-1H-indole, N-BOC protected, tert-Butyl 5-(2-chloroethyl)-2,3-dihydro-1H-indole-1-carboxylate, 1-(tert-Butoxycarbonyl)-5-(2-chloroethyl)-2,3-dihydro-1H-indole
CAS 860024-94-8

860024-94-8 - Physico-chemical Properties

Molecular FormulaC15H20ClNO2
Molar Mass281.78
Boling Point410.2±30.0 °C
Storage Condition2-8°C

860024-94-8 - Introduction

1H-Indole-1-carboxylic acid, 5-(2-chloroethyl)-2,3-dihydro-, 1,1-dimethyleyl ester is an organic compound whose structural formula is:

It is an indoline derivative containing chloroethyl and N-Boc protecting groups. The following is a detailed description of its nature, use, preparation and safety information:

Nature:
-Appearance: 1H-Indole-1-carboxylic acid, 5-(2-chloroethyl)-2,3-dihydro-, 1,1-dimethanol ester is a solid, usually white to light yellow crystals.
-Melting point: According to literature reports, its melting point range is 85-88 degrees Celsius.
-Solubility: It is soluble in some organic solvents, such as ethanol, dimethylformamide (DMF) and dichloromethane.

Use:
1H-indole-1-carboxylic acid, 5-(2-chloroethyl)-2,3-dihydro-, 1,1-dimethylethyl ester has certain application value in organic synthesis and can be used to construct the structure of indoline compounds. It acts as an intermediate compound that can be further converted into other organic compounds by reaction.

Preparation Method:
The specific details of the preparation method may be different. The following is a reference preparation method:
1H-Indole-1-carboxylic acid, 5-(2-chloroethyl)-2,3-dihydro-, 1,1-dimethylethyl ester can be obtained by reacting 5-chloroacetyl chloride with N-Boc-indoline under alkaline conditions. The reaction is generally carried out in a suitable solvent and at low temperature. After the reaction, steps such as purification and crystallization are required.

Safety Information:
Because the safety of a chemical depends on factors such as its specific quality, purity, and conditions of use, consult a reliable chemical database or relevant literature for detailed safety information and operational measures before using or operating the chemical. At the same time, it is recommended to follow correct laboratory safety procedures and use personal protective equipment when conducting chemical experiments or operations.
Last Update:2024-04-09 21:04:16
860024-94-8
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Shanghai Amole Biotechnology Co., Ltd.
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Product Name: tert-Butyl5-(2-chloroethyl)indoline-1-carboxylate Request for quotation
CAS: 860024-94-8
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Product Name: 1H-Indole-1-carboxylic acid, 5-(2-chloroethyl)-2,3-dihydro-, 1,1-diMethylethyl ester Visit Supplier Webpage Request for quotation
CAS: 860024-94-8
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Shanghai Amole Biotechnology Co., Ltd.
Spot supply
Product Name: tert-Butyl5-(2-chloroethyl)indoline-1-carboxylate Request for quotation
CAS: 860024-94-8
Tel: 400-968-2212
Email: 3623107365@qq.com
Mobile: 18916960931
QQ: 3623107365 Click to send a QQ message
Wechat: 18916960931
Shanghai Yuanye Bio-Technology Co., Ltd.
Product Name: 1H-Indole-1-carboxylic acid, 5-(2-chloroethyl)-2,3-dihydro-, 1,1-diMethylethyl ester Visit Supplier Webpage Request for quotation
CAS: 860024-94-8
Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
QQ: 3008007409 Click to send a QQ message
View History
860024-94-8
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