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3709-08-8

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3709-08-8 Usage

General Description

Alpha,alpha-dimethyl-gamma-butyrolactone, also known as dihydro-2(3H)-furanone, is a chemical compound with the molecular formula C6H10O2. It is a colorless liquid with a characteristic fruity odor and is used as a flavoring agent in the food industry. It is also used in the production of pharmaceuticals and as a solvent in various chemical processes. Alpha,alpha-dimethyl-gamma-butyrolactone is considered to be relatively safe for use in food and pharmaceutical applications, with no known adverse health effects at typical exposure levels. However, it should be handled with care and proper safety precautions, as it is flammable and may cause irritation to the skin and eyes.

Check Digit Verification of cas no

The CAS Registry Mumber 3709-08-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,0 and 9 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3709-08:
(6*3)+(5*7)+(4*0)+(3*9)+(2*0)+(1*8)=88
88 % 10 = 8
So 3709-08-8 is a valid CAS Registry Number.
InChI:InChI=1/C6H10O2/c1-6(2)3-4-8-5(6)7/h3-4H2,1-2H3

3709-08-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name α,α-DIMETHYL-γ-BUTYROLACTONE

1.2 Other means of identification

Product number -
Other names Dihydro-3,3-dimethyl-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:3709-08-8 SDS

3709-08-8Relevant articles and documents

HIGHLY REGIOSELECTIVE RING-OPENING OF α-SUBSTITUTED CYCLIC ACID ANHYDRIDES CATALYZED BY LIPASE

Hiratake, Jun,Yamamoto, Kazuyoshi,Yamamoto, Yukio,Oda, Jun'ichi

, p. 1555 - 1556 (2007/10/02)

Lipase Amano P irreversibly catalyzed a ring-opening of α-substituted cyclic acid anhydrides 1 preferentially at the less hindered carbonyl group to give monoesters with high regioselectivity.

Regio- and Stereoselective Dehydrogenation of α,ω-Diols Catalyzed by a Rhodium Hydride Complex

Ishii, Youichi,Suzuki, Katsumi,Ikariya, Takao,Saburi, Masahiko,Yoshikawa, Sadao

, p. 2822 - 2824 (2007/10/02)

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CATALYTIC REGIOSELECTIVE DEHYDROGENATION OF UNSYMMETRICAL α,ω-DIOLS USING RUTHENIUM COMPLEXES

Ishii, Youichi,Osakada, Kohtaro,Ikariya, Takao,Saburi, Masahiko,Yoshikawa, Sadao

, p. 2677 - 2680 (2007/10/02)

Ruthenium complex catalyzed regioselective dehydrogenation of unsymmetrically substituted 1,4- and 1,5-diols in the presence of α,β-unsaturated ketone as a hydrogen acceptor and triethylamine gave β-substituted γ-lactones and γ-substituted δ-lactones as major products, respectively.

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