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10601-63-5

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10601-63-5 Usage

General Description

N-(propan-2-yl)propanamide, also known as isobutyramide, is a chemical compound with the formula C5H11NO. It is an amide, which is a derivative of carboxylic acid. It is commonly used as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. Isobutyramide has a variety of industrial applications, including as a solvent and a chemical intermediate in the production of other organic compounds. It is a colorless, odorless liquid at room temperature and is relatively stable under normal conditions. Isobutyramide is considered to be of low toxicity and is not known to cause any harmful effects on human health or the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 10601-63-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,6,0 and 1 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 10601-63:
(7*1)+(6*0)+(5*6)+(4*0)+(3*1)+(2*6)+(1*3)=55
55 % 10 = 5
So 10601-63-5 is a valid CAS Registry Number.

10601-63-5SDS

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-propan-2-ylpropanamide

1.2 Other means of identification

Product number -
Other names Propanamide,N-isopropyl

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:10601-63-5 SDS

10601-63-5Relevant articles and documents

Aminolysis of N-Acylpyrazoles

Kashima, Choji,Fukuchi, Iwao,Takahashi, Katsumi,Hosomi, Akira

, p. 1407 - 1412 (2007/10/02)

1-Acylpyrazoles reacted with amines having a tiny substituted to afford the corresponding amides.The aminolysis with bulky amines was controlled to be retarded by the steric factors.Due to this steric interaction, the stereoselective aminolysis was observed.This selectivity of aminolysis should increase the utility of pyrazoles as auxiliary compounds in the synthetic loop.

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