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Propanoic acid, 2,2-dimethyl-, 2-methoxyphenyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

25491-51-4

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25491-51-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 25491-51-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,4,9 and 1 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 25491-51:
(7*2)+(6*5)+(5*4)+(4*9)+(3*1)+(2*5)+(1*1)=114
114 % 10 = 4
So 25491-51-4 is a valid CAS Registry Number.

25491-51-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-methoxyphenyl) 2,2-dimethylpropanoate

1.2 Other means of identification

Product number -
Other names o-Methoxyphenylpivalat

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:25491-51-4 SDS

25491-51-4Relevant academic research and scientific papers

Palladium-Catalyzed Esterification of Carboxylic Acids with Aryl Iodides

Kitano, Hiroyuki,Ito, Hideto,Itami, Kenichiro

supporting information, p. 2428 - 2432 (2018/04/27)

The first palladium-catalyzed esterification of carboxylic acids with aryl iodides is described. A palladium-based catalytic system consisting of IBnF (1,3-bis((pentafluorophenyl)methyl)imidazole-2-ylidene) ligand was found to significantly acc

Cyanation of Phenol Derivatives with Aminoacetonitriles by Nickel Catalysis

Takise, Ryosuke,Itami, Kenichiro,Yamaguchi, Junichiro

supporting information, p. 4428 - 4431 (2016/10/12)

Generation of useful arylnitrile structures from simple aromatic feedstock chemicals represents a fundamentally important reaction in chemical synthesis. The first nickel-catalyzed cyanation of phenol derivatives with metal-free cyanating agents, aminoacetonitriles, is described. A nickel-based catalytic system consisting of a unique diphosphine ligand such as dcype or dcypt enables the cyanation of versatile phenol derivatives such as aryl carbamates and aryl pivalates. The use of aminoacetonitriles as a cyanating agent leads to an environmentally and easy-to-use method for arylnitrile synthesis.

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