37029-36-0 Usage
Description
(4-oxo-3-p-tolyl-3,4-dihydro-quinazolin-2-ylsulfanyl)-acetic acid hydrazine is a complex organic compound with a quinazoline core and a hydrazine group. It also contains a sulfanyl group, which may contribute to its reactivity and biological activity. (4-oxo-3-p-tolyl-3,4-dihydro-quinazolin-2-ylsulfanyl)-acetic acid hydrazine has potential pharmaceutical applications and could be used as a drug candidate or a building block for synthesizing other bioactive molecules.
Uses
Used in Pharmaceutical Industry:
(4-oxo-3-p-tolyl-3,4-dihydro-quinazolin-2-ylsulfanyl)-acetic acid hydrazine is used as a potential drug candidate due to its unique structural features and potential biological activity. Its quinazoline core and hydrazine group are important structural motifs in medicinal chemistry, and the presence of a sulfanyl group may enhance its reactivity and interactions with biological targets.
Used in Drug Synthesis:
(4-oxo-3-p-tolyl-3,4-dihydro-quinazolin-2-ylsulfanyl)-acetic acid hydrazine can be used as a building block for synthesizing other bioactive molecules. Its complex structure and functional groups make it a promising starting point for the development of new drugs with potential therapeutic applications.
Further research and testing would be needed to fully understand the properties and potential applications of (4-oxo-3-p-tolyl-3,4-dihydro-quinazolin-2-ylsulfanyl)-acetic acid hydrazine. Its unique structural features and potential reactivity make it an interesting compound for exploration in the field of medicinal chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 37029-36-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,0,2 and 9 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 37029-36:
(7*3)+(6*7)+(5*0)+(4*2)+(3*9)+(2*3)+(1*6)=110
110 % 10 = 0
So 37029-36-0 is a valid CAS Registry Number.
37029-36-0Relevant articles and documents
Synthesis of methyl [3-alkyl-2-(2,4-dioxo-3,4-dihydro-2H-quinazolin-1-yl)-acetamido] alkanoate
Ismail, El Fekki,Ali, Ibrahim A.I.,Fathalla, Walid,Alsheikh, Amer A.,Tamney, El Said El
, p. 104 - 120 (2017/06/19)
A series of methyl [3-alkyl-2-(2,4-dioxo-3,4-dihydro-2H-quinazolin-1-yl)-acetamido] alkanoate 10-13a-f has been developed on the basis of the N-chemoselective reaction of 3-substituted quinazoline-2,4-diones 3a-d with ethyl chloroacetate and azide coupling method with amino acid ester hydrochloride. The precursor quinazoline diones 3a-d chemoselective reactions were studied using DFT(B3LYP)/6-311G level of theory and were prepared by a new rearrangement method from the corresponding 2-(3-methyl-4-oxo-3,4- dihydroquinazolin-2-ylthio) acetohydrazide 6. {figure presented}.
Synthesis and biological activities of 4-oxo thiazolidine derivatives
Sanghani,Sanja,Rajani,Godhani
experimental part, p. 557 - 560 (2009/08/07)
A series of 4-oxo-2-phenyl-thiazolidin-3-yl derivatives 5a-l have been obtained by cyclisation of various Schiff's base 4 with thioglycolic acid. The Schiff's base 4 are obtained by the reaction of appropriate carbonyl compound with (4-oxo-3-p-tolyl-3,4-dihydro-quinazolin-2-yl-sulfanyl)-acetic acid hydrazide 3. The product is characterized by spectral and analytical data. Most of the tested compounds show promising antibacterial and antifungal activity.
