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Benzenemethanol, 2-(methylamino)-α-(4-nitrophenyl)-, also known as 2-(methylamino)-α-(4-nitrophenyl)benzenemethanol, is an organic compound with the chemical formula C14H14N2O3. It is a derivative of benzenemethanol, featuring a methylamino group at the 2-position and a 4-nitrophenyl group at the α-position. Benzenemethanol, 2-(methylamino)-a-(4-nitrophenyl)- is characterized by its yellow crystalline appearance and is soluble in organic solvents such as ethanol and acetone. It is primarily used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of certain pesticides and drugs. Due to its reactivity and potential applications, it is important to handle this chemical with care, adhering to proper safety protocols.

61327-29-5

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61327-29-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61327-29-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,3,2 and 7 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 61327-29:
(7*6)+(6*1)+(5*3)+(4*2)+(3*7)+(2*2)+(1*9)=105
105 % 10 = 5
So 61327-29-5 is a valid CAS Registry Number.

61327-29-5SDS

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 2-methyl-2-(alpha-hydroxybenzyl)aniline

1.2 Other means of identification

Product number -
Other names (2-Methylamino-phenyl)-(4-nitro-phenyl)-methanol

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:61327-29-5 SDS

61327-29-5Downstream Products

61327-29-5Relevant academic research and scientific papers

Carbon Dioxide: A Reagent for the Simultaneous Protection of Nucleophilic Centres and the Activation of Alternative Locations to Electrophilic Attack. Prt III. A New Synthetic Method for the ortho-Substitution of N-Monoalkylanilines

Katritzky, Alan R.,Fan, Wei-Qiang,Akutagawa, Kunihiko

, p. 4027 - 4034 (2007/10/02)

N-Methyl- and N-ethyl-aniline are regiospecifically converted into a range of ortho-substituted derivatives, using carbon dioxide both for N-protection and as an intermediate carbanion stabilizing group, and t-butyllithium to lithiate the ortho-carbon atom.The rersulting lithium N-(ortho-substituted-phenyl)-N-methyl- and -N-ethylcarbamates undergo smooth acid-catalysed decarboxylation under mild conditions.No alpha-substituted products were detected.

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