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22458-07-7

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22458-07-7 Usage

General Description

2-[(4-chlorobutanoyl)amino]benzamide is a chemical compound with the molecular formula C11H13ClN2O2. It is a derivative of benzamide and contains a butanoyl group attached to the amino group of the benzamide. The compound is classified as an amide, which is a functional group that contains a carbonyl group bonded to a nitrogen atom. The presence of the 4-chloro substituent on the butanoyl group adds additional complexity to the compound's chemical structure. 2-[(4-chlorobutanoyl)amino]benzamide may have various applications in chemical and pharmaceutical industries but should be handled with care due to its potentially hazardous properties.

Check Digit Verification of cas no

The CAS Registry Mumber 22458-07-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,4,5 and 8 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 22458-07:
(7*2)+(6*2)+(5*4)+(4*5)+(3*8)+(2*0)+(1*7)=97
97 % 10 = 7
So 22458-07-7 is a valid CAS Registry Number.

22458-07-7SDS

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 2-(4-chlorobutanoylamino)benzamide

1.2 Other means of identification

Product number -
Other names N-(2-benzamido)-4-chlorobutanamide

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:22458-07-7 SDS

22458-07-7Relevant articles and documents

On the Synthesis and Reactivity of 2,3-Dihydropyrrolo[1,2- a ]quinazolin-5(1 H)-ones

Sutherell, Charlotte L.,Ley, Steven V.

supporting information, p. 135 - 144 (2016/12/24)

An improved, scalable synthetic route to the quinazolinone natural product 2,3-dihydropyrrolo[1,2-a]quinazolin-5(1H)-one is reported. The applicability of this method to analogue synthesis and the synthesis of related natural products is explored. Finally, reactivity of the scaffold to a variety of electrophilic reagents, generating products stereoselectively, is reported.

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