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α-Nitro-p-chloroisobutyrophenone is an organic compound with the chemical formula C10H10ClNO3. It is a derivative of isobutyrophenone, featuring a nitro group (-NO2) at the alpha (α) position and a chloro group (-Cl) at the para (p) position on the phenyl ring. This yellow crystalline solid is known for its potential use as a chemical intermediate in the synthesis of various pharmaceuticals and agrochemicals. Due to its reactivity and the presence of functional groups, it is typically handled with care in a controlled laboratory environment.

74261-44-2

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74261-44-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74261-44-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,2,6 and 1 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 74261-44:
(7*7)+(6*4)+(5*2)+(4*6)+(3*1)+(2*4)+(1*4)=122
122 % 10 = 2
So 74261-44-2 is a valid CAS Registry Number.

74261-44-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name α-nitro-p-chloroisobutyrophenone

1.2 Other means of identification

Product number -
Other names -

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

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More Details:74261-44-2 SDS

74261-44-2Relevant academic research and scientific papers

1-BENZYL-1,4-DIHYDRONICOTINAMIDE AS A REAGENT FOR REPLACING ALIPHATIC NITRO GROUPS BY HYDROGEN. AN ELECTRON-TRANSFER CHAIN REACTION.

Ono,Tamura,Kaji

, p. 4017 - 4022 (1983)

The reaction of alpha -nitro nitriles, alpha -nitro esters, and alpha -nitro ketones with 1-benzyl-1,4-dihydronicotinamide (BNAH) can occur with selective replacement of the nitro group by hydrogen without affecting other functional groups. Evidence is presented to support the claim that the reaction proceeds via an electron-transfer chain mechanism in which radical anions and free radicals are intermediates.

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