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Valeric acid, 3-(chloroformyl)-4-hydroxy-4-methyl-, gamma-lactone (6CI) is a chemical compound with the molecular formula C6H9ClO3. It is a derivative of valeric acid, featuring a chloroformyl group at the 3-position, a hydroxyl group at the 4-position, and a methyl group also at the 4-position. The gamma-lactone structure indicates the presence of a lactone ring, which is a cyclic ester formed from the intramolecular esterification of the carboxylic acid group with a hydroxyl group. Valeric acid, 3-(chloroformyl)-4-hydroxy-4-methyl-, gamma-lactone (6CI) is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, particularly as an intermediate in the production of certain drugs and pesticides. Its unique structure allows for further chemical modifications, making it a valuable building block in organic chemistry.

98546-95-3

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98546-95-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 98546-95-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,5,4 and 6 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 98546-95:
(7*9)+(6*8)+(5*5)+(4*4)+(3*6)+(2*9)+(1*5)=193
193 % 10 = 3
So 98546-95-3 is a valid CAS Registry Number.

98546-95-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2-dimethyl-5-oxooxolane-3-carbonyl chloride

1.2 Other means of identification

Product number -
Other names 3-Furancarbonylchloride,tetrahydro-2,2-dimethyl-5-oxo

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:98546-95-3 SDS

98546-95-3Upstream product

98546-95-3Downstream Products

98546-95-3Relevant academic research and scientific papers

Synthesis and pharmacological study of some new β-(dialkylaminomethyl)-γ-butyrolactones and their tetrahydrofuran analogues

Foscolos,Kolocouris,Fytas,Marakos,Pouli,Vamvakides

, p. 19 - 26 (2007/10/03)

This paper describes the synthesis of β-(dialkylaminomethyl)-γ-butyrolactones (6 and 15) and their tetrahydrofuran analogs 7 and 16. Their convulsant activity was studied on mice and could display an antiGABAergic component, but, unlike the α-(dialkylamin

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