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7180-62-3

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7180-62-3 Usage

General Description

4-methoxy-5-methylcyclopent-4-ene-1,3-dione exhibits both cyclic and carbonyl characteristics, contributing to its diverse chemical properties. With a molecular weight of 140.14 g/mol, it is a relatively small organic molecule. The methoxy group introduces a methoxy substituent (-OCH3), adding specific chemical reactivity to the overall structure. 4-methoxy-5-methylcyclopent-4-ene-1,3-dione may find applications in organic synthesis, potentially serving as a building block or intermediate in the creation of more complex molecules with diverse functionalities.

Check Digit Verification of cas no

The CAS Registry Mumber 7180-62-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,8 and 0 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 7180-62:
(6*7)+(5*1)+(4*8)+(3*0)+(2*6)+(1*2)=93
93 % 10 = 3
So 7180-62-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H8O3/c1-4-5(8)3-6(9)7(4)10-2/h3H2,1-2H3

7180-62-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-methoxy-5-methylcyclopent-4-ene-1,3-dione

1.2 Other means of identification

Product number -
Other names 3-Methoxy-3-methyl-cyclopent-2-en-1,4-dion

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:7180-62-3 SDS

7180-62-3Relevant articles and documents

A New Approach to Rethrolone Synthesis

Jondiko, Isaac J. O.,Pattenden, Gerald

, p. 467 - 470 (2007/10/02)

Rearrangement of the 4-ylidenebutenolides (4) and (5), with sodium methoxide in methanol, leads to the cyclopent-2-ene-1,4-diones (6), which when heated with sodium chloride in dimethyl sulphoxide give the 1,4-diones (7).The latter can be reduced using zinc in acetic acid, to the dihydroethrolones (8).In a similar manner, rearrangement of (10) produces (11a) which can be demethoxycarbonylated to (11b), an intermediate used previously in a synthesis of natural jasmololone (8; R = EtCH:CH).

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