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Benzoic acid, 4-chloro-, 2,2-dimethylhydrazide, also known as 4-chlorobenzoic acid 2,2-dimethylhydrazide, is a chemical compound with the molecular formula C9H11ClN2O2. It is a derivative of benzoic acid, where a chlorine atom is attached to the 4th carbon position, and a 2,2-dimethylhydrazide group is attached to the carboxylic acid group. This white crystalline solid is primarily used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. The compound is known for its potential applications in the development of antimicrobial agents and other therapeutic compounds. Due to its reactivity and chemical properties, it is essential to handle Benzoic acid, 4-chloro-, 2,2-dimethylhydrazide with care, following proper safety protocols to minimize health and environmental risks.

3902-82-7

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3902-82-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3902-82-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,9,0 and 2 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3902-82:
(6*3)+(5*9)+(4*0)+(3*2)+(2*8)+(1*2)=87
87 % 10 = 7
So 3902-82-7 is a valid CAS Registry Number.

3902-82-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-chloro-benzoic acid N',N'-dimethyl-hydrazide

1.2 Other means of identification

Product number -
Other names 4-Chlor-α',α'-dimethylhydrazid

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:3902-82-7 SDS

3902-82-7Relevant academic research and scientific papers

N-Ammonium Ylide Mediators for Electrochemical C-H Oxidation

Saito, Masato,Kawamata, Yu,Meanwell, Michael,Navratil, Rafael,Chiodi, Debora,Carlson, Ethan,Hu, Pengfei,Chen, Longrui,Udyavara, Sagar,Kingston, Cian,Tanwar, Mayank,Tyagi, Sameer,McKillican, Bruce P.,Gichinga, Moses G.,Schmidt, Michael A.,Eastgate, Martin D.,Lamberto, Massimiliano,He, Chi,Tang, Tianhua,Malapit, Christian A.,Sigman, Matthew S.,Minteer, Shelley D.,Neurock, Matthew,Baran, Phil S.

supporting information, p. 7859 - 7867 (2021/05/26)

The site-specific oxidation of strong C(sp3)-H bonds is of uncontested utility in organic synthesis. From simplifying access to metabolites and late-stage diversification of lead compounds to truncating retrosynthetic plans, there is a growing need for new reagents and methods for achieving such a transformation in both academic and industrial circles. One main drawback of current chemical reagents is the lack of diversity with regard to structure and reactivity that prevents a combinatorial approach for rapid screening to be employed. In that regard, directed evolution still holds the greatest promise for achieving complex C-H oxidations in a variety of complex settings. Herein we present a rationally designed platform that provides a step toward this challenge using N-ammonium ylides as electrochemically driven oxidants for site-specific, chemoselective C(sp3)-H oxidation. By taking a first-principles approach guided by computation, these new mediators were identified and rapidly expanded into a library using ubiquitous building blocks and trivial synthesis techniques. The ylide-based approach to C-H oxidation exhibits tunable selectivity that is often exclusive to this class of oxidants and can be applied to real-world problems in the agricultural and pharmaceutical sectors.

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