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612480-60-1

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612480-60-1 Usage

Uses

4,4''-Dihydroxybiphenyl-d8 (rings-d8) (CAS# 612480-60-1) is a useful isotopically labeled research compound.

Check Digit Verification of cas no

The CAS Registry Mumber 612480-60-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,1,2,4,8 and 0 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 612480-60:
(8*6)+(7*1)+(6*2)+(5*4)+(4*8)+(3*0)+(2*6)+(1*0)=131
131 % 10 = 1
So 612480-60-1 is a valid CAS Registry Number.

612480-60-1SDS

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 4,4'-dihydroxybiphenol-d8

1.2 Other means of identification

Product number -
Other names 4,4'-DIHYDROXYBIPHENYL-D8

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:612480-60-1 SDS

612480-60-1Upstream product

612480-60-1Downstream Products

612480-60-1Relevant articles and documents

Study of the ferroelectric liquid crystal 11EB1M7 by means of 2NMR

Catalano, Donata,Chiezzi, Leonardo,Domenici, Valentina,Geppi, Marco,Veracini, Carlo Alberto

, p. 10104 - 10113 (2003)

In this work, a new procedure for the synthesis of the selectivity deuterium-labeled chiral liquid crystal (+)-(S)-4-[4′-(1-methylheptyloxy)] biphenyl 4(10-undecenylox)benzoate (11EB1M7) has been developed, aimed to the study of its structure, orientational ordering, and dynamic behavior by means of 2H NMR. 11EB1M7 was investigated throughout its mesophasic range, formed by a very rich variety of chiral liquid crystalline phases including blue, cholesteric, TGBA*, and smectic C*. Two isotopomers were synthesized by labeling 11EB1M7 on either the phenyl or the biphenyl moiety of the mesogenic core. This allowed structural information (such as the tilt angle of the rigid fragments of the molecule and the angle between their para axes), orientational order parameters, and individual diffusional coefficients for the various overall and internal motions to be obtained from 2H NMR spectra and relaxation measurements by applying suitable data analyses based on several theoretical models.

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