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19792-52-0

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19792-52-0 Usage

Chemical compound

2-Amino-2-butylhexanol (ABD)

Class

Amine

Uses

Manufacturing of pharmaceuticals, reagent in organic synthesis

Structure

Butyl chain and amino group

Value

Intermediate for production of various compounds

Potential

Building block for synthesis of drugs and organic molecules

Applications

Stabilizer, additive in industrial products like lubricants and plasticizers
Wide range of applications in pharmaceutical and chemical industries

Check Digit Verification of cas no

The CAS Registry Mumber 19792-52-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,7,9 and 2 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 19792-52:
(7*1)+(6*9)+(5*7)+(4*9)+(3*2)+(2*5)+(1*2)=150
150 % 10 = 0
So 19792-52-0 is a valid CAS Registry Number.

19792-52-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-amino-2-butylhexan-1-ol

1.2 Other means of identification

Product number -
Other names diethylethanolamine

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:19792-52-0 SDS

19792-52-0Relevant articles and documents

A Short Access to Symmetrically α,α-Disubstituted α-Amino Acids from Acyl Cyanohydrins

Boukattaya, Fatma,Caillé, Julien,Ammar, Houcine,Rouzier, Florian,Boeda, Fabien,Pearson-Long, Morwenna S. M.,Bertus, Philippe

, p. 906 - 916 (2016/03/12)

A straightforward synthesis of symmetrically α,α-disubstituted α-amino acids is presented. The key step of this process relies on the efficient double addition of Grignard reagents to acyl cyanohydrins to provide N-acyl amino alcohols selectively in good yields. The chemoselectivity of the reaction was modulated by the nature of the acyl moiety. Eleven amino acids were prepared, including the particularly simple divinylglycine, which is not easily accessible by using conventional methods.

Tricyclic oxazolidone derivatives useful as PR modulators

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Page/Page column 16, (2008/06/13)

Compounds of the following structure are described: wherein R1-R6, R16, m, V, W, X, Y, and Q are described herein, or a pharmaceutically acceptable salt, tautomer, metabolite or prodrug thereof. These compounds are use

Oxazolidine derivatives as PR modulators

-

Page/Page column 15, (2010/11/30)

Compounds of the following structure are described: wherein R1-R6, m, V, W, X, Y, Z and Q are described herein, or a pharmaceutically acceptable salt, tautomer, metabolite or prodrug thereof. These compounds are useful for treating a

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