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N-ACETYL-6-HYDROXY-N-HEXYLAMINE) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

23363-92-0

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23363-92-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 23363-92-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,3,6 and 3 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 23363-92:
(7*2)+(6*3)+(5*3)+(4*6)+(3*3)+(2*9)+(1*2)=100
100 % 10 = 0
So 23363-92-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H17NO2/c1-8(11)9-6-4-2-3-5-7-10/h10H,2-7H2,1H3,(H,9,11)

23363-92-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(6-hydroxyhexyl)acetamide

1.2 Other means of identification

Product number -
Other names N-Acetyl-6-hydroxyhexylamine

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:23363-92-0 SDS

23363-92-0Downstream Products

23363-92-0Relevant academic research and scientific papers

Oxime esters as acylating agents in the aminolysis reaction. A simple and chemoselective method for the preparation of amides from amino alcohols

Fernandez,Menendez,Gotor

, p. 713 - 716 (2007/10/02)

Oxime esters, such as acetone O-alkanoyl-, O-alkenoyl- or O-benzyloxycarbonyloximes, react with amines under extremely mild conditions to give the corresponding amides in very good yield. When amino alcohols are used a total chemoselectivity is observed.

A USEFUL METHOD FOR SELECTIVE ACYLATION OF ALCOHOLS USING 2,2'-BIPYRIDYL-6-YL CARBOXYLATE AND CESIUM FLUORIDE

Mukaiyama, Teruaki,Pai, Fong-Chang,Onaka, Makoto,Narasaka, Koichi

, p. 563 - 566 (2007/10/02)

Primary and secondary alcohols are acylated under mild conditions by the of use 2,2'-bipyridyl-6-yl carboxylates and cesium fluoride.Furthermore, the reaction is successfully applied to selective acylation of a primary carbinol group of diols containing primary and secondary carbinol groups or exclusive O-acylation of aromatic amino alcohols.

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