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Pentanoic acid 4-formylphenyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

50262-50-5

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50262-50-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 50262-50-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,2,6 and 2 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 50262-50:
(7*5)+(6*0)+(5*2)+(4*6)+(3*2)+(2*5)+(1*0)=85
85 % 10 = 5
So 50262-50-5 is a valid CAS Registry Number.
InChI:InChI=1/C12H14O3/c1-2-3-4-12(14)15-11-7-5-10(9-13)6-8-11/h5-9H,2-4H2,1H3

50262-50-5SDS

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 (4-formylphenyl) pentanoate

1.2 Other means of identification

Product number -
Other names Pentanoic acid,4-formylphenyl 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:50262-50-5 SDS

50262-50-5Relevant academic research and scientific papers

Rhodium-Catalyzed Carbonylative Coupling of Alkyl Halides with Phenols under Low CO Pressure

Ai, Han-Jun,Li, Chong-Liang,Wang, Hai,Wu, Xiao-Feng

, p. 5147 - 5152 (2020/05/27)

A rhodium-catalyzed carbonylative transformation of alkyl halides under low pressure of CO has been developed. This robust catalyst system allows using phenols as the carbonylative coupling partner and, meanwhile, exhibits high functional group tolerance and good chemoselectivity. Substrates even with a large steric hindrance group or multiple reaction sites can be selectively converted into the desired products in good to excellent yields. A gram-scale experiment was performed and delivered an almost quantitative amount of the product. Control experiments were performed as well, and a possible reaction mechanism is proposed.

Synthesis, Structure, and Mesomorphic Properties of 2,5-Disubstituted 1,3-Dioxanes

Novikova,Sidel'nikova,Galatina

, p. 727 - 730 (2007/10/03)

New 5-alkyl-2-[4-(2-haloalkanoyloxy)phenyl]-1,3-dioxanes were synthesized. Pure trans isomers of these compounds were isolated, whose structure was confirmed by 1H and 13C NMR spectroscopy. Factors influencing mesogenic properties of the products are discussed.

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