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5-methyl-3-(prop-2-en-1-yl)dihydrofuran-2(3H)-one is a complex organic compound with the molecular formula C8H12O2. It features a dihydrofuran ring, which is a partially saturated furan ring, with a methyl group at the 5-position and a prop-2-en-1-yl group at the 3-position. The compound has a 3H-diketone structure, indicating the presence of two carbonyl groups. This chemical is known for its unique structure and potential applications in the synthesis of various organic compounds and pharmaceuticals. Its properties, such as reactivity and stability, are influenced by the presence of the dihydrofuran ring and the substituents attached to it.

3926-76-9

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3926-76-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3926-76-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,9,2 and 6 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3926-76:
(6*3)+(5*9)+(4*2)+(3*6)+(2*7)+(1*6)=109
109 % 10 = 9
So 3926-76-9 is a valid CAS Registry Number.

3926-76-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-methyl-3-prop-2-enyloxolan-2-one

1.2 Other means of identification

Product number -
Other names 3-Allyldihydro-5-methyl-2(3H)-furanone

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:3926-76-9 SDS

3926-76-9Relevant academic research and scientific papers

Enantiospecific Preparation of the Lactone Fragment of Murisolin

Harmange, Jean-Christophe,Figadere, Bruno,Hocquemiller, Reynald

, p. 347 - 350 (2007/10/02)

Both enantiomers (R) and (S) of the functionalized unsaturated γ-lactone moiety of the acetogenin murisolin have been enantiospecifically synthezised from L and D-glutamic acid respectively.

Photochemical degradation of barbituric acid derivatives. Part 4: Kinetics and TLC investigations of photolysis of proxibarbal

Mokrosz,Zurowska,Bojarski

, p. 832 - 835 (2007/10/02)

The photodegradation of proxibarbal in aqueous solution at different pH values by kinetic and TLC methods was studied. Rate constants, Arrhenius and thermodynamic parameters and pK[a] values were determined. The kinetic model of proxibarbal photolysis was proposed.

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