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680182-18-7

4-BENZYLOXY-[7-13C]BENZYL ALCOHOL is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

680182-18-7

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680182-18-7 Usage

Chemical Properties

Solid

Check Digit Verification of cas no

The CAS Registry Mumber 680182-18-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,8,0,1,8 and 2 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 680182-18:
(8*6)+(7*8)+(6*0)+(5*1)+(4*8)+(3*2)+(2*1)+(1*8)=157
157 % 10 = 7
So 680182-18-7 is a valid CAS Registry Number.
InChI:InChI=1/C14H14O2/c15-10-12-6-8-14(9-7-12)16-11-13-4-2-1-3-5-13/h1-9,15H,10-11H2/i10+1

680182-18-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Benzyloxy-[7-13C]benzyl Alcohol

1.2 Other means of identification

Product number -
Other names 4-(benzyloxy)-benzyl-[1-13C]-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:680182-18-7 SDS

680182-18-7Relevant articles and documents

Synthesis of [3,4,8-13C3]daidzein

Oldfield, Mark F.,Chen, Lirong,Botting, Nigel P.

, p. 1887 - 1893 (2007/10/03)

The biological effects of the soy isoflavones have attracted considerable interest in recent years leading to numerous studies on dietary intake and epidemiology. Such studies require accurate and reproducible analytical methods. Herein we report the firs

SYNTHESIS OF 13C-LABELLED ESTROGEN ANALOGUES

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Page 55-56, (2010/02/08)

There is provided a method of producing novel 13C-labelled estrogen analogues. The method preferably proceeds via an intermediate A or B or which is a mixture of (A) or (B): wherein a13C atom is located at one or more of positions 1, 2, 3 or 4 and wherein R is an optionally substituted alkane, alkene, alkyne or aryl group. Preferably R is -CH2Ph. An alternative preferred intermediate compound is 13C-resorcinol.

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