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Benzene, 5-(bromomethyl)-1,2-dimethoxy-3-(phenylmethoxy)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

651340-08-8

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651340-08-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 651340-08-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,5,1,3,4 and 0 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 651340-08:
(8*6)+(7*5)+(6*1)+(5*3)+(4*4)+(3*0)+(2*0)+(1*8)=128
128 % 10 = 8
So 651340-08-8 is a valid CAS Registry Number.

651340-08-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(bromomethyl)-1,2-dimethoxy-3-phenylmethoxybenzene

1.2 Other means of identification

Product number -
Other names 3-(benzyloxy)-4,5-dimethoxybenzyl bromide

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:651340-08-8 SDS

651340-08-8Relevant academic research and scientific papers

Biosynthesis of yatein in Anthriscus sylvestris.

Sakakibara, Norikazu,Suzuki, Shiro,Umezawa, Toshiaki,Shimada, Mikio

, p. 2474 - 2485 (2007/10/03)

Little is known about the biosynthesis of yatein, in spite of its importance as a typical heartwood lignan and a key biosynthetic intermediate of the antitumor lignan podophyllotoxin. The present study, based on individual administration of [13C]phenylalanine and deuterium labelled lignans and simultaneous administration of two distinct lignans labelled with deuterium atoms to Anthriscus sylvestris, established the two independent branch pathways from matairesinol, one to afford yatein via thujaplicatin, 5-methylthujaplicatin, and 4,5-dimethylthujaplicatin and the other to bursehernin via pluviatolide. The latter pathway did not lead to yatein, eliminating the presence of a metabolic grid from matairesinol to yatein.

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