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1,3,4-Oxadiazole-2(3H)-thione, 5-[4-methyl-2-phenyl-5-(1H-pyrrol-1-yl)thieno[2,3-d]pyrimidin-6-yl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

487005-31-2

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487005-31-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 487005-31-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,8,7,0,0 and 5 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 487005-31:
(8*4)+(7*8)+(6*7)+(5*0)+(4*0)+(3*5)+(2*3)+(1*1)=152
152 % 10 = 2
So 487005-31-2 is a valid CAS Registry Number.

487005-31-2Relevant academic research and scientific papers

Synthesis and structure of novel thieno[2,3-d]pyrimidine derivatives containing 1,3,4-oxadiazole moiety

Ho, Yuh-Wen,Suen, Maw-Cherng

experimental part, p. 408 - 415 (2009/12/06)

The reaction of 5-(1-pyrrolyl)-4-methyl-2-phenylthieno[2,3-d]pyrimidine carbohydrazide 5 with CS2 in the presence of pyridine afforded the 6-(2,3-dihydro-2-mercapto-1,3,4-oxadiazol-5-yl)-4-methyl-5-(1-pyrrolyl) -2-phenylthieno[2,3-d]pyrimidine

Synthesis and reactions of some new thienopyrimidines

Moneam, Maisa I. Abdel,Geies, Ahmed A.,El-Naggar, Galal M.,Mussa, Suliman M.

, p. 737 - 751 (2007/10/03)

4-Methyl-6-mercapto-2-phenylpyrimidine-5-carbonitrile (1) was reacted with different halo compounds, namely ethylchloroacetate, chloroacetone, bromoacetanilide, p-chlorobromoacetanilide, and p-methoxy chloroacetanilide in ethanol in the presence of sodium acetate yielded the corresponding S-alkylated derivatives (2a-e). The latter compounds underwent cyclization into thienopyrimidines (4a-e) upon treatment with sodium ethoxide in ethanol. The reaction of (4a) with hydrazine hydrate led to the formation of 5-amino-4-methyl-2-phenylthieno[2,3-d]pyrimidine-2-carbohydrazide (5). Compound (5) was reacted with a variety of reagents to produce other new thienopyrimidines as well as oxadiazolylthienopyrimidines (6, 11).

Synthesis of novel pyrrylthieno-[2,3-d]pyrimidines and related pyrrolo[1″,2″:1′,6′]pyrazino-[2′,3′:4,5] thieno[2,3-d]pyrimidines

Bakhite,Geies,El-Kashef

, p. 303 - 323 (2007/10/03)

4-Methyl-2-phenyl-5-(1-pyrryl)-6-substituted-thieno[2,3-d]pyrimidines (3a-c, 4a-c, 5a,b, and 6) have been synthesized. Some of the substituents in position 6 were used to build up different sulfur-, nitrogen-and/or oxygen-containing heterocyclic rings at that position. The 4-methyl- 2-phenyl-5-(1-pyrryl)-thieno[2,3-d]pyrimidine-6-carboazide (20) was also used as a key intermediate in the synthesis of the target pyrrolo[1″,2″:1′,6′]pyrazino[2′,3′:4, 5/thieno[2,3-d]pyrimidines.

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