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Benzene, 1,2,3-trimethoxy-5-(4-methoxyphenoxy)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

112221-36-0

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112221-36-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 112221-36-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,2,2 and 1 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 112221-36:
(8*1)+(7*1)+(6*2)+(5*2)+(4*2)+(3*1)+(2*3)+(1*6)=60
60 % 10 = 0
So 112221-36-0 is a valid CAS Registry Number.

112221-36-0SDS

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 1,2,3-trimethoxy-5-(4-methoxyphenoxy)benzene

1.2 Other means of identification

Product number -
Other names Benzene,1,2,3-trimethoxy-5-(4-methoxyphenoxy)

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:112221-36-0 SDS

112221-36-0Relevant academic research and scientific papers

Antimitotic and cell growth inhibitory properties of combretastatin A-4-like ethers

Lawrence, Nicholas J.,Rennison, David,Woo, Meiki,McGown, Alan T.,Hadfield, John A.

, p. 51 - 54 (2001)

A series of diarylamines, diaryl and arylbenzyl ethers based on combretastatin A-4 was prepared and evaluated for anticancer activity. 2-Methoxy-5-(3',4',5'-trimethoxyphenoxymethyl)phenol was the most active (IC50, K562 20 nM) and caused significant G2/M cell cycle arrest. (C) 2000 Elsevier Science Ltd.

Antibiotics from Algae, 38. - Base-Catalyzed Reactions of Multiple Hydroxylated Diphenyl Ethers

Glombitza, Karl-Werner,Woelwer-Rieck, Ursula

, p. 261 - 266 (2007/10/02)

Diphenyl ethers are in general difficult to cleave.Under certain conditions in a weak alkaline aqueous solution multiple hydroxylated diphenyl ethers are brought to reaction.It is shown at 33 model substances which substitution pattern must be present in

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