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2-methylphenyl 4-chlorobenzoate is an organic compound with the chemical formula C14H11ClO2. It is a derivative of benzoic acid, featuring a 4-chloro substituent on the benzene ring and a 2-methyl substituent on the phenyl group. 2-methylphenyl 4-chlorobenzoate is characterized by its aromatic structure and exhibits properties typical of esters, such as reactivity with nucleophiles and the ability to undergo hydrolysis. It is used in the synthesis of various pharmaceuticals and agrochemicals due to its potential to form complex molecular structures. The compound is also known for its potential applications in materials science, particularly in the development of new polymers and coatings. Its chemical structure and reactivity make it a valuable intermediate in organic synthesis, highlighting its importance in the field of chemistry.

6280-50-8

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6280-50-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6280-50-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,8 and 0 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6280-50:
(6*6)+(5*2)+(4*8)+(3*0)+(2*5)+(1*0)=88
88 % 10 = 8
So 6280-50-8 is a valid CAS Registry Number.

6280-50-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-methylphenyl) 4-chlorobenzoate

1.2 Other means of identification

Product number -
Other names 4-chloro-benzoic acid o-tolyl ester

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:6280-50-8 SDS

6280-50-8Relevant academic research and scientific papers

TETRAZOLINONE COMPOUND AND APPLICATIONS THEREOF

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Paragraph 0833; 0860, (2015/11/24)

Disclosed is a tetrazolinone compound having a high pest control effect and represented by the formula (1): wherein R1, R2, R3, and R11 each represent a halogen atom, a C1-C6 alkyl group, or the like; R4 and R5 each represent a hydrogen atom, a halogen atom, a C1-C3 alkyl group, or the like; R6 represents a C1-C3 alkyl group which may have a halogen atom(s) or the like; R7, R8, and R9 each represent a hydrogen atom, a halogen atom, or the like; R10 represents a C1-C3 alkyl group or the like; R12 represents a C1-C6 alkyl group, a C3-C6 cycloalkyl group, or the like, and R13 represents a C1-C6 alkyl group, a C2-C6 alkenyl group, or the like.

N-Heterocyclic carbene catalysed aerobic oxidation of aromatic aldehydes to aryl esters using boronic acids

Arde, Panjab,Ramanjaneyulu,Reddy, Virsinha,Saxena, Apurv,Anand, R. Vijaya

supporting information; experimental part, p. 848 - 851 (2012/02/05)

The organocatalytic behavior of N-heterocyclic carbenes in the aerobic oxidation of aromatic aldehydes to esters with boronic acids has been explored. This transition metal-free protocol allows access to a wide variety of aromatic esters in good to excellent yields under mild reaction conditions.

A novel photochemical Wittig reaction for the synthesis of 2-aryl/alkylbenzofurans

Ghosh, Somnath,Das, Jhantu

scheme or table, p. 1112 - 1116 (2011/03/22)

The synthesis of 2-aryl/alkylbenzofurans has been achieved in high yields under photochemical conditions from readily accessible and suitably substituted phosphonium bromides by an intramolecular photochemical Wittig reaction onto aryloxycarbonyl groups.

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