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Benzoic acid, 4-methoxy-, 2-(hydroxymethyl)-1,4-phenylene ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

105252-91-3

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105252-91-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 105252-91-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,2,5 and 2 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 105252-91:
(8*1)+(7*0)+(6*5)+(5*2)+(4*5)+(3*2)+(2*9)+(1*1)=93
93 % 10 = 3
So 105252-91-3 is a valid CAS Registry Number.

105252-91-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,5-bis[(4'-(methoxy)benzoyl)oxy]benzyl alcohol

1.2 Other means of identification

Product number -
Other names 2,5-bis(4-methoxybenzoyloxy)benzyl alcohol

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:105252-91-3 SDS

105252-91-3Downstream Products

105252-91-3Relevant academic research and scientific papers

Liquid crystal polymers copolymers and elastomers containing a laterally attached mesogenic unit

Whale, Eric A.,Davis, Frederick J.,Mitchell, Geoffrey R.

, p. 1479 - 1485 (1996)

The synthesis of a closely-coupled laterally attached side-chain liquid crystal polymer is described. The material exhibits liquid crystalline behaviour over a wide temperature range. Incorporation of non-mesogenic methyl acrylate as a comonomer with the

Selective reduction of 2-[(benzoyl)oxy]benzaldehydes without intramolecular transesterification

Pugh, Coleen

, p. 1329 - 1331 (2000)

(equation presented) NaBH4 reduction of 2,5-bis[(4′-(n-alkoxy)benzoyl)oxy]benzaldehydes produces primarily the rearranged phenol, which does not generate liquid crystalline phases when laterally attached to a polymer backbone. Rearrangement is prevented by quenching the intermediate benzyl alkoxide with a weak acid. For example, 2,5-bis[(4′-(methoxy)benzoyl)oxy]benzaldehyde is selectively reduced to 2,5-bis[(4′-(methoxy)benzoyl)oxy]-benzyl alcohol with less than 5% intramolecular transesterification using 2-3 equiv of NaBH4 in the presence of 20-30 equiv of acetic acid (1:10 NaBH4/AcOH).

Synthesis of 2,5-(4-alkoxybenzoyloxy)benzyl acrylates and cinnamates, monomers for side chain liquid crystal polymers

Li, Yong,Yuan, Yao,Yang, Yu-Guo,Li, Zhi

, p. 63 - 71 (2017/01/14)

Abstract: A variety of 2,5-(4-alkoxybenzoyloxy)benzyl acrylates and cinnamates, which can serve as monomers for side chain liquid crystal polymers, were readily synthesized from hydroquinone. Instead of the rare and expensive 2,5-dihydroxybenzaldehyde, ch

SYNTHESIS OF A NEW CLASS OF SIDE CHAIN LIQUID CRYSTAL POLYMERS. POLYMERS WITH MESOGENS LATERALLY ATTACHED VIA SHORT LINKAGES TO POLYMER BACKBONES

Zhou, Qi-Feng,Li, Hui-Min,Feng, Xin-De

, p. 73 - 82 (2007/10/02)

New monomers, 2,5-(4-alkoxybenzoyloxy)benzyl acrylates were synthesized.Upon radical polymerizations of these monomers thermotropic liquid crystalline polyacrylates with mesogens laterally attached to polymer backbones via short linkages were obtained.The

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