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6170-23-6

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6170-23-6 Usage

Formation

Salt formed by reaction of 2-aminopropan-1-ol with hydrochloric acid

Uses

Reagent in organic synthesis and pharmaceutical research

Physical properties

Colorless, odorless solid at room temperature; highly soluble in water

Biological activities

Anti-inflammatory and analgesic properties

Applications

Production of pharmaceutical drugs; potential treatment for medical conditions

Check Digit Verification of cas no

The CAS Registry Mumber 6170-23-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,7 and 0 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6170-23:
(6*6)+(5*1)+(4*7)+(3*0)+(2*2)+(1*3)=76
76 % 10 = 6
So 6170-23-6 is a valid CAS Registry Number.
InChI:InChI=1/C3H9NO.ClH/c1-3(4)2-5;/h3,5H,2,4H2,1H3;1H

6170-23-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name dl-2-amino-1-propanol hydrochloride

1.2 Other means of identification

Product number -
Other names 1-Propanol, 2-amino-, hydrochloride

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:6170-23-6 SDS

6170-23-6Relevant articles and documents

Radical-mediated intramolecular β-C(sp3)-H amidation of alkylimidates: Facile synthesis of 1,2-amino alcohols

Mou, Xue-Qing,Chen, Xiang-Yu,Chen, Gong,He, Gang

supporting information, p. 515 - 518 (2018/01/19)

A new radical-mediated intramolecular β-C(sp3)-H amidation reaction of O-alkyl trichloro- or arylimidates is reported. Various oxazolines were efficiently prepared from easily accessible alcohol starting materials. The trichloro-oxazoline products can be hydrolyzed under mild conditions to give valuable 1,2-amino alcohols. This amidation reaction exhibits a broad substrate scope and good functional group tolerance, and offers a powerful means for the C(sp3)-H functionalization of alcohols. Mechanistic studies suggest that a sequence of 1,5-HAT of an imidate radical, iodination and cyclization might be operative.

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