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
3709-08-8Relevant 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.