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898746-54-8

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898746-54-8 Usage

General Description

2-(4-Chloro-1H-indol-3-yl)ethanol, N-BOC protected is a chemical compound that consists of a chloroindole ring attached to an ethanol group, with the nitrogen atom of the indole ring protected by a tert-butoxycarbonyl (N-BOC) group. 2-(4-Chloro-1H-indol-3-yl)ethanol, N-BOC protected is commonly used in organic synthesis and medicinal chemistry as a versatile building block for the creation of complex molecules. The N-BOC protection on the indole nitrogen atom helps to prevent unwanted reactions during chemical synthesis, allowing for greater control over the reaction process. The presence of the chloro group on the indole ring also provides opportunities for further chemical modifications, making this compound valuable for the production of diverse molecular structures with potential pharmaceutical applications.

Check Digit Verification of cas no

The CAS Registry Mumber 898746-54-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,8,7,4 and 6 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 898746-54:
(8*8)+(7*9)+(6*8)+(5*7)+(4*4)+(3*6)+(2*5)+(1*4)=258
258 % 10 = 8
So 898746-54-8 is a valid CAS Registry Number.

898746-54-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl 4-chloro-3-(2-hydroxyethyl)indole-1-carboxylate

1.2 Other means of identification

Product number -
Other names 2-(4-Chloro-1H-indol-3-yl)ethanol,N-BOC protected

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:898746-54-8 SDS

898746-54-8Downstream Products

898746-54-8Relevant articles and documents

Enantioselective Halocyclization of Indole Derivatives: Using 1,3-Dihalohydantoins with Anionic Chiral Co(III) Complexes

Sun, Ting-Ting,Liu, Kun,Zhang, Shun-Xin,Wang, Chun-Ru,Yao, Chuan-Zhi,Yu, Jie

supporting information, p. 701 - 707 (2021/01/21)

Highly enantioselective halocyclization reactions of indole derivatives, including tryptophols and tryptamines, have been accomplished by means of anionic chiral Co(III) complexes and 1,3-dihalohydantoins (as little as 0.50 equiv). 3-Halo-fused indolines

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