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2-nitrophenyl 4-methylbenzoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

36718-35-1

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36718-35-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 36718-35-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,7,1 and 8 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 36718-35:
(7*3)+(6*6)+(5*7)+(4*1)+(3*8)+(2*3)+(1*5)=131
131 % 10 = 1
So 36718-35-1 is a valid CAS Registry Number.

36718-35-1SDS

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 2-nitrophenyl 4-methylbenzoate

1.2 Other means of identification

Product number -
Other names p-Methylbenzoesaeure-o-nitrophenylester

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:36718-35-1 SDS

36718-35-1Relevant academic research and scientific papers

2-substituted benzoxazole preparation method of compound

-

Paragraph 0052, (2016/10/20)

The invention relates to a preparing method of 2-substituted benzoxazole compounds. The compounds are obtained by reaction of products obtained by reaction of acyl chloride and o-nitrophenol or derivatives thereof under catalyzing of reducing agent ammonium formate, a solvent and palladium-containing agents. According to the method, the reaction condition is mild, environment is protected, raw materials are rich and easy to obtain, operation is easy, yield is high, and various kinds of performance are optimized.

A convenient procedure for the esterification of benzoic acids with phenols: a new application for the Mitsunobu reaction

Fitzjarrald, Victor P.,Pongdee, Rongson

, p. 3553 - 3557 (2008/02/06)

The Mitsunobu reaction was found to be a convenient and effective method for the esterification of various benzoic acids with differentially functionalized phenols producing the corresponding phenyl esters in good to excellent yields.

Photolysis of 2-Nitrophenyl Benzyl Ethers in Neutral and Acidic Media

Jacob E. Dominic,Joshua, C. P.

, p. 808 - 810 (2007/10/02)

2-Nitrophenyl benzyl ethers (1a-d) on irradiation afford N-benzoyl-2-aminophenols (4) as the major products.The other minor products are 2-nitrophenol (2), 4-benzyl-2-nitrophenol (3), 2-phenylbenzoxazoles (5) and 2-nitrophenyl benzoate (6).A plausible mechanism to account for the formation of various products is discussed.

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