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(Z)-3-(3-Phenyl-3H-[1,2,3]triazolo[4,5-d]pyrimidin-7-yloxy)-but-2-enoic acid ethyl ester is a complex organic compound with the molecular formula C19H16N4O3. It is characterized by a phenyl group attached to a triazolo[4,5-d]pyrimidine core, which is further connected to a but-2-enoic acid moiety through an ethyl ester linkage. This molecule exhibits a (Z)-configuration, indicating the geometric arrangement of the double bond in the but-2-enoic acid chain. It is a derivative of a triazolo[4,5-d]pyrimidine, a heterocyclic compound with potential applications in medicinal chemistry, particularly as a building block for the development of new drugs. The ethyl ester group suggests that (Z)-3-(3-Phenyl-3H-[1,2,3]triazolo[4,5-d]pyrimidin-7-yloxy)-but-2-enoic acid ethyl ester may be used in prodrug strategies, where it can be hydrolyzed in vivo to release the active carboxylic acid form.

74529-00-3

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74529-00-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74529-00-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,5,2 and 9 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 74529-00:
(7*7)+(6*4)+(5*5)+(4*2)+(3*9)+(2*0)+(1*0)=133
133 % 10 = 3
So 74529-00-3 is a valid CAS Registry Number.

74529-00-3Downstream Products

74529-00-3Relevant academic research and scientific papers

Triazolopyrimidines. V. The Nucleophilic Substitution of 7-Chloro- and 7-(p-Tolylsulfonyl)-3-phenyl-3H-1,2,3-triazolopyrimidines

Higashino, Takeo,Katori, Tatsuhiko,Kawaraya, Hideji,Hayashi, Eisaku

, p. 337 - 343 (2007/10/02)

The substitution reaction of 7-chloro- (1) and 7-(p-tolylsulfonyl)-3-phenyl-3H-1,2,3-triazolopyrimidines (2) with various nucleophiles (NuH or Nu(-)) was carried out.The reaction of 1 with amines (NuH-1 to NuH-11) gave 7-(N-substituted amino)-3-phe

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