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Benzene, 1,1'-(2-methylpropylidene)bis[2,5-dimethoxy- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

89950-14-1

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89950-14-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89950-14-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,9,5 and 0 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 89950-14:
(7*8)+(6*9)+(5*9)+(4*5)+(3*0)+(2*1)+(1*4)=181
181 % 10 = 1
So 89950-14-1 is a valid CAS Registry Number.

89950-14-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[1-(2,5-dimethoxyphenyl)-2-methylpropyl]-1,4-dimethoxybenzene

1.2 Other means of identification

Product number -
Other names -

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:89950-14-1 SDS

89950-14-1Downstream Products

89950-14-1Relevant academic research and scientific papers

Three-component synthesis of 3,4-dihydroisoquinoline derivatives

Shklyaev, Yu. V.,Nifontov, Yu. V.

, p. 844 - 849 (2007/10/03)

A simple and convenient method for the synthesis of 1-substituted 3,3-dimethyl-3,4-dihydroisoquinolines was developed. The method is based on the [2+2+2] cyclization of alkyl- or alkoxybenzenes with isobutyraldehyde and nitriles.

DIMETHOXY AROMATIC COMPOUNDS. II. BROMODEALKYLATION REACTIONS OF meta-DIMETHOXYBENZENE DERIVATIVES

Natoli, Maria C.,Agozzino, Pasquale,Ceraulo, Leopoldo,Lamartina, Liliana

, p. 493 - 502 (2007/10/02)

Comparison of the behaviour of 1,1-bis(dimethoxyphenyl)ethane derivatives towards bromination in different experimental conditions shows that only 2,4-dimethoxy derivatives undergo bromodealkylation processes, the aromatic displacement of the arylethane group occurring only when a high electron density resides at the alkyl-substituted carbon

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