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121086-26-8

4-Benzyloxy-5-methoxy-2-nitrotoluene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

121086-26-8

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121086-26-8 Usage

Chemical Properties

Yellow Needles

Uses

A substituted nitrotoluene.

Check Digit Verification of cas no

The CAS Registry Mumber 121086-26-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,1,0,8 and 6 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 121086-26:
(8*1)+(7*2)+(6*1)+(5*0)+(4*8)+(3*6)+(2*2)+(1*6)=88
88 % 10 = 8
So 121086-26-8 is a valid CAS Registry Number.

121086-26-8SDS

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 1-methoxy-5-methyl-4-nitro-2-phenylmethoxybenzene

1.2 Other means of identification

Product number -
Other names 2-Nitro-5-methoxy-4-benzyloxy-toluol

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:121086-26-8 SDS

121086-26-8Relevant articles and documents

IRAK DEGRADERS AND USES THEREOF

-

Paragraph 2654; 2656, (2019/07/10)

The present invention provides compounds, compositions thereof, and methods of using the same.

Isomeric Monomethyl Ether Derivatives of (RS)-9,10-Dihydroxyaporphine ("Isoapomorphine") as Possible Products of Metabolism by Catechol-O-methyltransferase

Cannon, Joseph G.,Qijie, Pang

, p. 1079 - 1082 (2007/10/02)

The isomeric monomethyl ether derivatives of (RS)-9,10-dihydroxyaporphine ("isoapomorphine") were synthesized unequivocally as possible metabolites in catechol-O-methyltransferase (COMT) mediated O-methylation reactions.In vitro incubation studies revealed that isoapomorphine is not a substrate for the COMT using experimental conditions under which apomorphine (10,11-dihydroxyaporphine) is converted in high yield into its 10-methyl ether, apocodeine.The in vivo dopaminergic inactivity of isoapomorphine (as compared with that of apomorphine) seems to be due to factors other than metabolic inactivation by COMT.

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