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1523-12-2

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1523-12-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1523-12-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,2 and 3 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1523-12:
(6*1)+(5*5)+(4*2)+(3*3)+(2*1)+(1*2)=52
52 % 10 = 2
So 1523-12-2 is a valid CAS Registry Number.

1523-12-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-nitrophenyl) benzoate

1.2 Other means of identification

Product number -
Other names Benzoicacid,2-nitrophenyl 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:1523-12-2 SDS

1523-12-2Relevant articles and documents

Tropolonate salts as acyl-transfer catalysts under thermal and photochemical conditions: Reaction scope and mechanistic insights

Mai, Binh Khanh,Koenigs, Rene M.,Nguyen, Thanh Vinh,Lyons, Demelza J.M.,Empel, Claire,Pace, Domenic P.,Dinh, An H.

, p. 12596 - 12606 (2020/11/18)

Acyl-transfer catalysis is a frequently used tool to promote the formation of carboxylic acid derivatives, which are important synthetic precursors and target compounds in organic synthesis. However, there have been only a few structural motifs known to efficiently catalyze the acyl-transfer reaction. Herein, we introduce a different acyl-transfer catalytic paradigm based on the tropolone framework. We show that tropolonate salts, due to their strong nucleophilicity and photochemical activity, can promote the coupling reaction between alcohols and carboxylic acid anhydrides or chlorides to give products under thermal or blue light photochemical conditions. Kinetic studies and density functional theory calculations suggest interesting mechanistic insights for reactions promoted by this acyl-transfer catalytic system.

2-substituted benzoxazole preparation method of compound

-

Paragraph 0024, (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.

Benzoyl peroxide-imidazole: A novel and efficient reagent for the mild conversion of alcohols or phenols into benzoates

Nowrouzi, Najmeh,Alizadeh, Seyedeh Zahra

, p. 2412 - 2414 (2013/06/26)

A very mild, one-pot, and expedient protocol for the conversion of alcohols and phenols into their corresponding benzoates using imidazole and benzoyl peroxide as a novel reagent is described.

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