114657-07-7 Usage
Molecular weight
338.41 g/mol
Type of compound
Thiobarbituric acid derivative of barbituric acid
Biological activity
Central nervous system depressant
Common use
Building block in organic synthesis and pharmaceutical research
Structural features
Presence of a phenyl and a methoxybenzyl group
Pharmacological properties
Influenced by the phenyl and methoxybenzyl groups
Potential applications
Medicinal applications due to unique molecular structure
Research interest
Subject of interest in medicinal chemistry and drug development research
Check Digit Verification of cas no
The CAS Registry Mumber 114657-07-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,6,5 and 7 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 114657-07:
(8*1)+(7*1)+(6*4)+(5*6)+(4*5)+(3*7)+(2*0)+(1*7)=117
117 % 10 = 7
So 114657-07-7 is a valid CAS Registry Number.
114657-07-7Relevant articles and documents
OXIDATION OF THIOL WITH 5-ARYLIDENE-1,3-DIMETHYLBARBITURIC ACID: APPLICATION TO SYNTHESIS OF UNSYMMETRICAL DISULFIDE
Tanaka, Kiyoshi,Chen, Xing,Yoneda, Fumio
, p. 3241 - 3250 (2007/10/02)
5-Arylidene-1,3-dimethylbarbituric acid derivatives, such as 1a and 1b, effectively oxidized both alkane- and benzenethiols to disulfides under neutral condition with concomitant formation of the dihydro compounds (2a) and (2b).Thiol adduct of the dihydro compound was prepared as a stable compound and successfully applied to the synthesis of unsymmetrical disulfide under mild condition in excellent yield.Mechanistic consideration for the oxidation was also described briefly.
