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6342-98-9

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6342-98-9 Usage

General Description

The chemical compound (4-methylphenyl)(2,3,4-trimethoxyphenyl)methanone is a ketone consisting of a 4-methylphenyl group and a 2,3,4-trimethoxyphenyl group attached to a carbonyl (C=O) functional group. It is derived from both methylphenol and trimethoxybenzene. (4-methylphenyl)(2,3,4-trimethoxyphenyl)methanone has potential applications in organic synthesis and pharmaceutical research due to its unique chemical structure and potential reactivity. Its specific properties and applications would depend on its use in various chemical reactions and processes.

Check Digit Verification of cas no

The CAS Registry Mumber 6342-98-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,4 and 2 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6342-98:
(6*6)+(5*3)+(4*4)+(3*2)+(2*9)+(1*8)=99
99 % 10 = 9
So 6342-98-9 is a valid CAS Registry Number.

6342-98-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-methylphenyl)-(2,3,4-trimethoxyphenyl)methanone

1.2 Other means of identification

Product number -
Other names HMS3088J20

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:6342-98-9 SDS

6342-98-9Downstream Products

6342-98-9Relevant articles and documents

Rapid microwave-promoted synthesis of functionalised benzophenones

Learmonth, David A.

, p. 2757 - 2762 (2002)

Several functionalised benzophenone derivatives have been conveniently obtained in moderate to good yield via the rapid, microwave-promoted Friedel-Crafts acylation of activated arenes with benzoic acids in polyphosphoric acid medium.

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