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140918-54-3

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140918-54-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 140918-54-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,0,9,1 and 8 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 140918-54:
(8*1)+(7*4)+(6*0)+(5*9)+(4*1)+(3*8)+(2*5)+(1*4)=123
123 % 10 = 3
So 140918-54-3 is a valid CAS Registry Number.

140918-54-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(8-prop-2-enoyloxyoctoxy)benzoic acid

1.2 Other means of identification

Product number -
Other names Benzoic acid,4-[[8-[(1-oxo-2-propenyl)oxy]octyl]oxy]

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:140918-54-3 SDS

140918-54-3Downstream Products

140918-54-3Relevant articles and documents

Hydrogen-bond induced side-chain liquid crystalline polymers based on nicotinic acid derivatives

Saravanan,Ambili,Kannan

, p. 217 - 222 (2011/10/18)

Supramolecular side-chain liquid crystalline poly(acrylate)s have been prepared by self-assembly of H-bond donor and acceptor complexes through intermolecular complementary hydrogen bond formation. Poly[4-(m-acryloyloxyalkyloxy)benzoic acid]s [m = 6 (P1) and 8 (P2)] were employed as polymer components. Liquid crystalline nicotinic acid derivatives (C1, C2, C3, and C4) were used as complementary H-bond donor/acceptor counterparts. The liquid crystalline properties of the nicotinic acid derivatives, the polymers and their complexes were investigated by DSC and POM. Methylene spacers present at the terminal position of the nicotinic acid derivatives played a key role in mesophase arrangements. The columnar phase exhibited by the nicotinic acid derivatives completely disappeared in the H-bonded complexes to afford a nematic phase, thereby substantiating the complex formation.

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