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N-(sec-butyl)-4-chlorobenzamide is a chemical compound with the molecular formula C11H14ClNO. It is a derivative of benzamide, featuring a 4-chloro substituent on the benzene ring and a sec-butyl group attached to the nitrogen atom. N-(sec-butyl)-4-chlorobenzamide is known for its potential applications in pharmaceuticals and agrochemicals, particularly as a precursor in the synthesis of various active ingredients. Its chemical structure endows it with specific properties that can be exploited in the development of new drugs or pesticides. The compound's stability, reactivity, and biological activity are key factors that determine its suitability for these applications.

7465-71-6

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7465-71-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7465-71-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,6 and 5 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 7465-71:
(6*7)+(5*4)+(4*6)+(3*5)+(2*7)+(1*1)=116
116 % 10 = 6
So 7465-71-6 is a valid CAS Registry Number.
InChI:InChI=1/C11H14ClNO/c1-3-8(2)13-11(14)9-4-6-10(12)7-5-9/h4-8H,3H2,1-2H3,(H,13,14)

7465-71-6SDS

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-butan-2-yl-4-chlorobenzamide

1.2 Other means of identification

Product number -
Other names 4-Chlor-N-sek.butyl-benzamid

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:7465-71-6 SDS

7465-71-6Downstream Products

7465-71-6Relevant academic research and scientific papers

N-acylbenzotriazoles: Neutral acylating reagents for the preparation of primary, secondary, and tertiary amides

Katritzky,He,Suzuki

, p. 8210 - 8213 (2000)

Readily available N-acylbenzotriazoles 2a-q efficiently acylate aqueous ammonia and primary and secondary amines to give primary, secondary, and tertiary amides in good to excellent yields. The wide applicability of the procedure is illustrated by the preparation of (i) α-hydroxyamides from α-hydroxy acids and of (ii) perfluoroalkylated amides.

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