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N-carbamoyl-2-ethylbutyraldehyde is an organic compound with the chemical formula C7H13NO2. It is a derivative of butyraldehyde, featuring a carbamoyl group (-CONH2) attached to the nitrogen atom. This aldehyde is characterized by a 2-ethylbutyraldehyde chain, which consists of a four-carbon chain with an ethyl group (-CH2CH3) attached to the second carbon. The molecule has a molecular weight of 143.19 g/mol and is known for its potential applications in the synthesis of various pharmaceuticals and chemical compounds. Due to its reactivity, it is often used as an intermediate in the production of drugs, agrochemicals, and other specialty chemicals.

2274-01-3

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2274-01-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2274-01-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,7 and 4 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2274-01:
(6*2)+(5*2)+(4*7)+(3*4)+(2*0)+(1*1)=63
63 % 10 = 3
So 2274-01-3 is a valid CAS Registry Number.

2274-01-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N-carbamoyl-2-ethylbutanamide

1.2 Other means of identification

Product number -
Other names EINECS 218-885-9

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:2274-01-3 SDS

2274-01-3Relevant academic research and scientific papers

PHOTOCHEMICAL RING OPENING OF BARBITAL

Barton, Henryk,Bojarski, Jacek,Mokrosz, Jerzy

, p. 2133 - 2134 (2007/10/02)

Photolysis of barbital yields derivatives of urea and biuret.The mechanism of ring opening involves an isocyanate intermediate.

Metabolism of bromocarbamides. I. In vitro degradation of carbromal and acetylcarbromal in rabbit liver

Sticht,Kaferstein

, p. 1021 - 1023 (2007/10/12)

10,000 g supernatant of rabbit liver homogenate catalyzes the deacetylation of acetylcarbromal to carbromal. Cis 2 ethyl crotonylurea was proved to be the in vitro debromination product. Trans 2 ethyl crotonylurea and 2 ethyl butyrylurea could be excluded to be primary metabolites of carbromal in this enzyme preparation by comparison of melting points and spectroscopic properties. N Acetyl 2 ethyl crotonylurea, a primary debromation product of acetylcarbromal, could not be detected.

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