6007-77-8 Usage
General Description
4-(2,5-DIMETHYLTHIEN-3-YL)-4-OXOBUTANOIC ACID is a chemical compound with the molecular formula C9H12O3S. It is a thienyl ketone derivative that contains a thienyl ring with two methyl substituents and a ketone group attached to a butanoic acid moiety. 4-(2,5-DIMETHYLTHIEN-3-YL)-4-OXOBUTANOIC ACID has potential therapeutic applications due to its ability to inhibit certain enzymes, such as dihydroorotate dehydrogenase, which are involved in important metabolic pathways. It is also being investigated for its potential use in the treatment of autoimmune diseases and certain types of cancers. Additionally, its unique structure and properties make it a valuable tool in chemical research and drug development.
Check Digit Verification of cas no
The CAS Registry Mumber 6007-77-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,0 and 7 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6007-77:
(6*6)+(5*0)+(4*0)+(3*7)+(2*7)+(1*7)=78
78 % 10 = 8
So 6007-77-8 is a valid CAS Registry Number.
InChI:InChI=1/C10H12O3S/c1-6-5-8(7(2)14-6)9(11)3-4-10(12)13/h5H,3-4H2,1-2H3,(H,12,13)
6007-77-8Relevant articles and documents
Efficient Hydrogenation of Biomass Oxoacids to Lactones by Using NHC–Iridium Coordination Polymers as Solid Molecular Catalysts
Liu, Yaoqi,Sun, Zheming,Huang, Changyu,Tu, Tao
, p. 355 - 360 (2017/02/05)
A series of NHC–iridium coordination polymers have proven to be robust, efficient and recyclable solid molecular catalysts toward the hydrogenation of biomass levulinic acid (LA) to γ-valerolactone. Along with quantitative yields attained at 0.01 mol % catalyst loading under 50 atm of H2, the solid molecular catalyst was readily recovered and reused for 12 runs without obvious loss of the selectivity and activity. Remarkably, up to 1.2×105 TON, an unprecedented value could be achieved in this important transformation. In addition, a number of LA homologues, analogues and derivatives were well tolerated to deliver various intriguing and functional lactones in good to excellent yields, which further confirmed the feasibility of the solid molecular catalysts.
