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69741-69-1

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69741-69-1 Usage

Description

Benzeneacetamide, 4-chloro-a-(1-methylethyl)-, also known as 4-chloro-α-isopropylbenzeneacetamide, is a chemical compound with the molecular formula C10H12ClNO. It is a derivative of benzeneacetamide, featuring a chlorine atom and an isopropyl group attached to the benzene ring. Benzeneacetamide, 4-chloro-a-(1-methylethyl)is commonly utilized as a reagent in organic synthesis and pharmaceutical research, and it exhibits analgesic and antipyretic properties, positioning it as a potential candidate for the development of new drugs. However, due to its potential health hazards, it is crucial to handle this chemical with care during its management and storage.

Uses

Used in Pharmaceutical Research:
Benzeneacetamide, 4-chloro-a-(1-methylethyl)is employed as a reagent in pharmaceutical research for its potential to contribute to the development of new drugs. Its analgesic and antipyretic properties make it a valuable compound for exploring its efficacy in treating pain and fever, respectively.
Used in Organic Synthesis:
In the field of organic synthesis, Benzeneacetamide, 4-chloro-a-(1-methylethyl)serves as a key intermediate for the synthesis of various organic compounds. Its unique structure, which includes a chlorine atom and an isopropyl group, allows for a range of chemical reactions that can lead to the formation of diverse molecules with different applications.

Check Digit Verification of cas no

The CAS Registry Mumber 69741-69-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,7,4 and 1 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 69741-69:
(7*6)+(6*9)+(5*7)+(4*4)+(3*1)+(2*6)+(1*9)=171
171 % 10 = 1
So 69741-69-1 is a valid CAS Registry Number.

69741-69-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-chlorophenyl)-3-methylbutyramide

1.2 Other means of identification

Product number -
Other names α-isopropyl-p-chlorophenylacetamide

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:69741-69-1 SDS

69741-69-1Relevant articles and documents

A novel class of potent influenza virus inhibitors: Polysubstituted acylthiourea and its fused heterocycle derivatives

Sun, Chuanwen,Huang, Hai,Feng, Meiqing,Shi, Xunlong,Zhang, Xiaodong,Zhou, Pei

, p. 162 - 166 (2007/10/03)

A series of polysubstituted and fused heterocycle derivatives of acylthiourea was prepared and the biological activity against influenza virus was evaluated. Of the analogues that demonstrated IC50s 0.1 μM, acylthiourea derivatives 16 and 50 were further investigated as candidates with the most potential for future development. The SAR of these compounds are discussed and they represent a novel class of highly potent and selective inhibitors of influenza virus.

Enantioselective Hydrolysis of (RS)-2-isopropyl-4'-chlorophenylacetonitrile by Pseudomonas sp. B21C9

Matsumoto, Shun-ichi,Inoue, Ayumu,Kumagai, Kazuo,Murai, Rika,Mitsuda, Satoshi

, p. 720 - 722 (2007/10/02)

Pseudomonal sp.B21C9, a new nitrile-degrading microorganism, was isolated from a soil sample.By a hydrolysis of (RS)-isopropyl-4'-chlorophenylacetonitrile using cells of B21C9, (S)-2-isopropyl-4'-chlorophenylacetic acid having excellent optically purity could be obtained.It appeared that the microbial hydrolysis proceeded via stepwise reactions by a nitrile hydratase having poor (S)-selectivity and an amidase having strict (S)-selectivity.

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