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1,1-Biphenyl,2,4-dimethoxy-6-methyl-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

92120-51-9

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92120-51-9 Usage

Structure

Aromatic compound with two phenyl rings connected by a single carbon-carbon bond

Methoxy groups

Two -OCH3 groups attached to the phenyl rings

Methyl group

One -CH3 group attached to the phenyl ring

Derivative

A derivative of biphenyl, a common organic compound found in various plant sources

Properties

Unique properties due to the presence of methoxy and methyl groups

Applications

Potential applications in organic synthesis and pharmaceutical research

Safety

Should be handled and used with caution, as its chemical properties and potential hazards should be thoroughly understood and evaluated before use

Chemical classification

9CI (Chemical Abstracts Service Registry Number)

Check Digit Verification of cas no

The CAS Registry Mumber 92120-51-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,1,2 and 0 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 92120-51:
(7*9)+(6*2)+(5*1)+(4*2)+(3*0)+(2*5)+(1*1)=99
99 % 10 = 9
So 92120-51-9 is a valid CAS Registry Number.

92120-51-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,5-dimethoxy-3-methyl-2-phenylbenzene

1.2 Other means of identification

Product number -
Other names 1,1-biphenyl,2,4-dimethoxy-6-methyl

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:92120-51-9 SDS

92120-51-9Downstream Products

92120-51-9Relevant academic research and scientific papers

Biomimetic Syntheses of Polyketide Aromatics from Pyrylium Salts

Griffin, David A.,Leeper, Finian J.,Staunton, James

, p. 1035 - 1042 (2007/10/02)

Following attack by nucleophiles, various methoxypyrylium compounds derived from 2H-pyran-2-ones and 4H-pyran-4-ones react either to produce a linear β-polycarbonyl derivative in which one or more carbonyl groups is derivatised in the form of an enol ether or to form a methylene-2H-pyran.The linear polycarbonyl derivatives can undergo biomimetic cyclisation to generate polyketide aromatic system; syntheses of the following benzene derivatives are described: ethyl 2,4-dimethoxy-6-methylbenzoate (29), 2,4-dimethoxy-6-methylbiphenyl (31), and 6-(2,4-dimethoxy-6-methylphenyl)- 4-methoxy-2H-pyran-2-one (34).

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