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Benzoic acid 4-[[(4-methoxyphenyl)methylene]amino]phenyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

16571-39-4

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16571-39-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16571-39-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,5,7 and 1 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 16571-39:
(7*1)+(6*6)+(5*5)+(4*7)+(3*1)+(2*3)+(1*9)=114
114 % 10 = 4
So 16571-39-4 is a valid CAS Registry Number.
InChI:InChI=1/C21H17NO3/c1-24-19-11-7-16(8-12-19)15-22-18-9-13-20(14-10-18)25-21(23)17-5-3-2-4-6-17/h2-15H,1H3/b22-15+

16571-39-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name [4-[(4-methoxyphenyl)methylideneamino]phenyl] benzoate

1.2 Other means of identification

Product number -
Other names 1-benzoyloxy-4-(4-methoxy-benzylidenamino)-benzene

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:16571-39-4 SDS

16571-39-4Downstream Products

16571-39-4Relevant academic research and scientific papers

Effects of Polysubstitution on Mesomorphic Properties: Chloro Derivatives of 4-Methoxyphenyl 4-(Phenyliminomethyl)benzoate and Related Compounds

Matsunaga, Y.,Yasuhara, K.

, p. 239 - 249 (2007/10/02)

The effects of mono-, di-, and trichloro substitution of one of the end phenyl rings upon the nematic-isotropic transition temperature have been studied employing seven three-ring systems with a terminal methoxyl group, in which the linkage groups are -CO-O- and -CH=N-.The transition temperatures in these compounds were mostly in this order: 4-Cl > 2,4-Cl2 > 2,3,4-Cl3 > 3,4-Cl2 > unsubstituted > 2,3-Cl2 > 2-Cl or 3-Cl.Both the substituents on the 2- and 3-positions drastically lowered the transition temperature of the parent compound and the extent of depression by the former substituent varied by a factor of more than two when the -CH=N- group nearby was inverted.The condition that the thermal stabilities of mesophases and the temperature ranges over which the mesophases exist must be considerable in a parent compound was not necessarily required for the appearance of an enantiotropic nematic-isotropic transition in laterally substituted derivatives.Keywords: Liquid crystals; nematic; smectic; lateral substituent

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