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37844-06-7

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37844-06-7 Usage

General Description

B-Amino-3-chlorobenzenepropanol is a chemical compound with a notable presence of nitrogen, chlorine, and hydroxyl groups. The presence of these groups suggests this compound may have the potential for a variety of reactions, such as acting as a base due to the amino group, or undergoing nucleophilic substitution or elimination due to the chlorine. It is composed of a benzene ring, a key component of many important chemicals, rendering it potentially useful in the synthesis of other chemical compounds. Detailed information about the hazards or possible uses of b-Amino-3-chlorobenzenepropanol is not widely available, suggesting it is not widely used or studied.

Check Digit Verification of cas no

The CAS Registry Mumber 37844-06-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,8,4 and 4 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 37844-06:
(7*3)+(6*7)+(5*8)+(4*4)+(3*4)+(2*0)+(1*6)=137
137 % 10 = 7
So 37844-06-7 is a valid CAS Registry Number.

37844-06-7SDS

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 2-Amino-3-(3-chlorphenyl)-propanol

1.2 Other means of identification

Product number -
Other names m-Chlorphenylalaninol

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:37844-06-7 SDS

37844-06-7Upstream product

37844-06-7Downstream Products

37844-06-7Relevant articles and documents

Nucleophilic RhI Catalyzed Selective Isomerization of Terminal Aziridines to Enamides

Tian, Yingying,Kunz, Doris

, p. 4272 - 4275 (2020/07/04)

The selective isomerization of various terminal N-Boc protected aziridines to enamides was realized using the highly reactive nucleophilic rhodium catalyst C with the Lewis acid LiNTf2 as co-catalyst under moderate conditions. The reaction proceeds smoothly with only 1 molpercent catalyst loading and excellent yields were achieved. An intermediate containing an enamide with a non-conjugated terminal C=C double bond was detected during the course of the reaction, which isomerizes to form the thermodynamically favored 2-amido styrene. Mechanistic insight is gained based on these observations.

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