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29040-33-3

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29040-33-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 29040-33-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,0,4 and 0 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 29040-33:
(7*2)+(6*9)+(5*0)+(4*4)+(3*0)+(2*3)+(1*3)=93
93 % 10 = 3
So 29040-33-3 is a valid CAS Registry Number.

29040-33-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-(2-formylphenoxy)propanoate

1.2 Other means of identification

Product number -
Other names -

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:29040-33-3 SDS

29040-33-3Relevant articles and documents

Biobased High-Performance Aromatic-Aliphatic Polyesters with Complete Recyclability

Cai, Zhongzheng,Fan, Hua-Zhong,Gong, Fu-Long,Tu, Yi-Min,Wang, Xue-Mei,Yang, Xing,Zhu, Jian-Bo

supporting information, p. 20591 - 20597 (2021/12/09)

The development of high-performance recyclable polymers represents a circular plastics economy to address the urgent issues of plastic sustainability. Herein, we design a series of biobased seven-membered-ring esters containing aromatic and aliphatic moie

Photocyclization Reactions. Part 2. Synthesis of Dihydrobenzofuranols Using Photocyclization of Ethyl 2-Formylphenoxyacetates and Ethyl 2-Acetylphenoxyacetates

Horaguchi, Takaaki,Tsukada, Chikara,Hasegawa, Eietsu,Shimizu, Takahachi,Suzuki, Tsuneo,Tanemura, Kiyoshi

, p. 1273 - 1280 (2007/10/02)

Photocyclization reactions were carried out on ethyl 2-formylphenoxyacetates 1a-e and ethyl 2-acetylphenoxyacetates 2a-e in acetonitrile.Irradiation of 1a-e gave dihydrobenzofuranols 3 in 20-46percent yields.Similarly, irradiation of 2a-e afforded dihydrobenzofuranols 6 and their derivatives 7, 8 in 40-86percent yields.Substitution effects on photocyclization and reaction pathways are discussed.

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