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114153-09-2

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114153-09-2 Usage

General Description

3,4-difluoro-2-methylaniline is a chemical compound that consists of a benzene ring with an amino group and two fluorine atoms attached at different positions. It is a derivative of aniline and is commonly used in the production of pharmaceuticals, agrochemicals, and dyes. 3,4-difluoro-2-methylaniline is known for its strong aromatic odor and is considered to be toxic when ingested or inhaled in high concentrations. 3,4-difluoro-2-methylaniline is also known to be a skin and eye irritant, and it should be handled with caution and proper protective equipment. Additionally, it is important to follow safety guidelines and regulations when working with this chemical to avoid any potential health hazards.

Check Digit Verification of cas no

The CAS Registry Mumber 114153-09-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,1,5 and 3 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 114153-09:
(8*1)+(7*1)+(6*4)+(5*1)+(4*5)+(3*3)+(2*0)+(1*9)=82
82 % 10 = 2
So 114153-09-2 is a valid CAS Registry Number.

114153-09-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,4-Difluoro-2-methylaniline

1.2 Other means of identification

Product number -
Other names Benzenamine,3,4-difluoro-2-methyl

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:114153-09-2 SDS

114153-09-2Relevant articles and documents

Ortho lithiation of N-pivaloylfluoroanilines as a useful tool for either selective methylation or benzoxazole synthesis

Yoshida, Yasuo,Hamada, Yusuke,Umezu, Kazuto,Tabuchi, Fumiya

, p. 958 - 961 (2004)

Lithiation of N-pivaloyl-3,4-difluoroaniline (1a) with a slight excess of 2 mole equiv of n-butyllithium followed by methylation was studied. The reaction was found to be useful for either the selective methylation of 3,4-difluoroaniline or the synthesis of benzoxazole derivatives, depending on the reaction temperature. In the reaction of N-pivaloyl-3-chloro-4-fluoroaniline (1b) and N-pivaloyl-3-fluoroaniline (1c), the reaction proceeded rather sluggishly but benzoxazole formation predominated.

A practical route to C-8 substituted fluoroquinolones

Carretero,Garcia Ruano,Vicioso

, p. 7373 - 7382 (2007/10/02)

The ortho metalation of N-(tert-butoxycarbonyl)-3,4-difluoroaniline, with t-BuLi at -78°C in THF occurred regioselectively at C-2 position. The resulting lithiated species reacted with a variety of electrophiles to give 2-substituted-3,4-difluoranilines i

1-Cyclopropyl-6-fluoro-7-piperazinyl-1,4-Dihydro-4-oxo-quinoline-3-carboxylic acid derivatives

-

, (2008/06/13)

Novel 4-oxoquinoline-3-carboxylic acid compounds of the formula: STR1 wherein R2 is a heterocyclic group: STR2 in which RA is H, C1 -C6 alkyl or phenyl (C1 -C6) alkyl, RB is 2-ox

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