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2597-54-8

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2597-54-8 Usage

General Description

Acetylurethane is a chemical compound also known as ethyl acetylurethane. It is a derivative of urethane and is used in the production of adhesives, coatings, and inks. Acetylurethane is known for its good solvent resistance and fast-drying properties. It is also used as a crosslinker in the production of polyurethane coatings and in the synthesis of pharmaceuticals and pesticides. Acetylurethane is classified as an organic compound and is commonly used in industrial applications due to its versatility and ability to improve the properties of various materials.

Check Digit Verification of cas no

The CAS Registry Mumber 2597-54-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,9 and 7 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2597-54:
(6*2)+(5*5)+(4*9)+(3*7)+(2*5)+(1*4)=108
108 % 10 = 8
So 2597-54-8 is a valid CAS Registry Number.
InChI:InChI=1/C5H9NO3/c1-3-9-5(8)6-4(2)7/h3H2,1-2H3,(H,6,7,8)

2597-54-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl N-acetylcarbamate

1.2 Other means of identification

Product number -
Other names Acetyl-urethan

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:2597-54-8 SDS

2597-54-8Relevant articles and documents

The photochemical addition of N-haloamides to olefins: a comparison of cyclic and acyclic N-halo-N-alkylamides and N-halo-N-acylamides (N-haloimides)

Lessard, Jean,Couture, Yvon,Mondon, Martine,Touchard, Daniel

, p. 105 - 112 (2007/10/02)

Upon photochemical decomposition in the presence of cyclohexene and 1-octene, an N-halo-N-acylamide (N-haloimide) leads to better yields of addition than its N-halo-N-alkyl analogue, and cyclic N-halo-N-alkyl and N-halo-N-acylamides add more efficiently than their acyclic analogues.The yields of addition were higher with N-chlorosuccinimide which has been added also to 1-methylcyclohexene than with N-bromosuccinimide which did not add to 1-methylcyclohexene.

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