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

65731-06-8

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65731-06-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65731-06-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,7,3 and 1 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 65731-06:
(7*6)+(6*5)+(5*7)+(4*3)+(3*1)+(2*0)+(1*6)=128
128 % 10 = 8
So 65731-06-8 is a valid CAS Registry Number.

65731-06-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-formylphenyl) 4-cyanobenzoate

1.2 Other means of identification

Product number -
Other names 4-(4'-cyanobenzoyloxy)benzaldehyde

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:65731-06-8 SDS

65731-06-8Relevant academic research and scientific papers

Effects of Branching of the Ester Alkyl Chain on the Mesomorphic Properties of Alkyl 4-benzoates

Matsuzaki, Hiroyuki,Matsunaga, Yoshio

, p. 2300 - 2305 (2007/10/02)

The mesomorphic properties of five homologous series of alkyl 4-benzoates, where X=CN, NO2, CH3, Cl, and CH3COO, have been studied.The ester alkyl groups employed were the following eleven types: ethyl and p

Liquid-Crystalline Heterocycloalkanes. III. Synthesis and Liquid-Crystalline Properties of Substituted 1,3-Dioxadecalines

Tschierske, C.,Zaschke, H.

, p. 1 - 14 (2007/10/02)

Liquid-crystalline 2-substituted and 2,6-disubstituted 1,3-dioxadecalines (4-6) were synthesized by acid-catalyzed acetalization of trans-2-hydroxymethylcyclohexanol (1) or trans-4-alkyl-trans-2-hydroxymethylcyclohexanoles (2) with aldehydes 3 whereby the desired trans-isomers were formed only.The syntheses of the various aldehydes are also described.Special attention is drawn on the evolution of mesogenic properties of the title compounds 4-6 in comparison with known decalines and 1,3-dioxanes.It was found that the clearing temperatures of the synthesized 1,3-dioxadecalines are always lower than those of the corresponding decaline derivatives, due to the deformation of the decaline-ringsystem by the introduction of two oxygen-atoms.The comparison of 1,3-dioxanes and 1,3-dioxadecalines shows that the dioxadecaline ringsystem tends to suppress smectic mesophases in favour of nematics.A first example of a liquid crystalline cis-fused 1,3-dioxadecaline (8) is described, too.

Quasi-Liquid Crystals of Thermochromic Spiropyrans. A Material Intermediate between Supercooled Liquids and Mesophases

Shvartsman, Felix P.,Krongauz, Valeri A.

, p. 6448 - 6453 (2007/10/02)

Crystals of thermochromic spiropyrans containing mesogenic groups give iosotropic melts.However, these materials from metastable films with mesogenic properties below the crystal melting points.A strong birefringence of the films appears concommitantly wi

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