6939-72-6 Usage
Description
6-oxo-6-propoxyhexanoic acid, also known as valproic acid, is a chemical compound with the molecular formula C8H16O3. It is a widely used medication for the management of epilepsy and bipolar disorder.
Used in Pharmaceutical Industry:
6-oxo-6-propoxyhexanoic acid is used as an anticonvulsant and mood-stabilizing drug for the treatment of epilepsy and bipolar disorder. It works by increasing the levels of certain neurotransmitters in the brain, which helps to control seizures and stabilize mood.
Used in Neurological Treatments:
6-oxo-6-propoxyhexanoic acid is used as a medication for managing neurological conditions such as epilepsy and bipolar disorder. It helps to control seizures and stabilize mood by increasing the levels of specific neurotransmitters in the brain.
Common side effects of 6-oxo-6-propoxyhexanoic acid include dizziness, drowsiness, and stomach upset, while more serious side effects such as liver damage and pancreatitis can occur with long-term use. It is available in various formulations, including tablets, capsules, and syrup, and is typically taken orally.
Check Digit Verification of cas no
The CAS Registry Mumber 6939-72-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,3 and 9 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6939-72:
(6*6)+(5*9)+(4*3)+(3*9)+(2*7)+(1*2)=136
136 % 10 = 6
So 6939-72-6 is a valid CAS Registry Number.
6939-72-6Relevant articles and documents
Synergism of microwaves and immobilized enzyme catalysis in synthesis of adipic acid esters in nonaqueous media
Yadav, Ganapati D.,Lathi, Piyush S.
, p. 1699 - 1705 (2007/10/03)
Low-energy microwave irradiation leads to enhancement by a factor of up to 2.63 in comparison with conventional heating in immobilized lipase-catalyzed esterification of adipic acid with various alcohols and this effect is due to the greater frequency of collision, without any change in activation energy of the two modes of heating. Copyright Taylor & Francis, Inc.
Convenient selective monoesterification of α, ω-dicarboxylic acids catalyzed by ion-exchange resins
Saitoh, Masahiko,Fujisaki, Shizuo,Ishii, Yasuhiro,Nishiguchi, Takeshi
, p. 6733 - 6736 (2007/10/03)
Symmetric dicarboxylic acids, ranging from pentanedioic acid to tetradecanedioic acid, gave selectively the corresponding monoesters in high yields in the transesterification catalyzed by strongly acidic ion-exchange resins in ester/octane mixtures.