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6-(Acetylamino)hexanamide is a chemical compound with the molecular formula C8H16N2O2. It is a white crystalline solid that is soluble in water and various organic solvents. 6-(Acetylamino)hexanamide is an amide derivative of 6-aminohexanoic acid, where the amino group is acylated with an acetyl group. It is used in the synthesis of various pharmaceuticals and chemical intermediates, particularly in the production of certain drugs and agrochemicals. Its unique structure allows for the formation of hydrogen bonds and other interactions, making it a versatile building block in organic chemistry.

2827-32-9

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2827-32-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2827-32-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,2 and 7 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2827-32:
(6*2)+(5*8)+(4*2)+(3*7)+(2*3)+(1*2)=89
89 % 10 = 9
So 2827-32-9 is a valid CAS Registry Number.

2827-32-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N-acetyl-ε-aminocapramide

1.2 Other means of identification

Product number -
Other names 6-Acetylamino-hexanoic acid amide

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:2827-32-9 SDS

2827-32-9Downstream Products

2827-32-9Relevant academic research and scientific papers

REACTION OF ε-CAPROLACTAM WITH AMIDES OF CARBOXYLIC ACIDS

Spasskaya, R. I.,Zil'berman, E. N.,Radina, I. A.

, p. 1809 - 1812 (2007/10/02)

ε-Caprolactam and the amides of carboxylic acids enter into a trans-amidation reaction with the formation of a mixture of N-acyl-ε-aminocapramides and the products from their subsequent transformations with ε-caprolactam.The N-acetyl- and N-benzoyl-ε-aminocapramides were synthesized at 225 deg C with an excess of the second agent.

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