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4-phenyl-6,7,8,9-tetrahydrobenzo[b]thieno[3,2-e]-1,2,4-triazolo[4,3-a]pyrimidin-1,5-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

142465-23-4

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142465-23-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 142465-23-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,2,4,6 and 5 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 142465-23:
(8*1)+(7*4)+(6*2)+(5*4)+(4*6)+(3*5)+(2*2)+(1*3)=114
114 % 10 = 4
So 142465-23-4 is a valid CAS Registry Number.

142465-23-4Downstream Products

142465-23-4Relevant academic research and scientific papers

Title studies on the reaction of N-(3-carbethoxy-4,5,6,7-tetrahydrobenzo[b] thien-2-yl)-N′-phenylthiourea with hydrazine hydrate (Part 1)

El-Sherief, Hassan A. H.,El-Naggar, Galal M.,Hozien, Zeinab A.,El-Sawaisi, Suliman M.

, p. 467 - 473 (2008/09/19)

(Chemical Equation Presented) The reaction of N-(3-carbethoxy-4,5,6,7- tetrahydrobenzo[b]thien-2-yl)-N′-phenylthiourea (1) with hydrazine hydrate in 1-butanol afforded a mixture of compounds 2, 3 and 4. Treatment of 3 and 4 with nitrous acid gave 6 and 8 respectively, while reactions of 3 with acetylacetone gave 7. Synthesis of tetracyclic compounds 9a-f and 11 from the reactions of 3 with ethyl orthoformate or appropriate acids, acid chloride, carbon disulphide and/or ethyl chloroformate. Also its reaction with isothiocyanate derivatives gave the corresponding thiosemicarbzides 12a,b which on, refluxing in alcoholic KOH gave the unexpected tetracyclic products 14a,b. Similarly the tetracyclic compounds 16a-e and 19 were obtained by cyclization of 4 and 18 respectively.

Synthesis of some triazolothienopyrimidin-5(4H)-ones

Pathak, U S,Gandhi, N V,Singh, S,Warde, R P,Jain, K S

, p. 223 - 229 (2007/10/02)

A series of hitherto unreported 1-(un)substituted-4-phenyltriazolothienopyrimidin-5(4H)-ones (8a-k) have been synthesized by the condensation of 2-hydrazino-3-phenylthienopyrimidin-4(3H)-ones (7a,b) with various one-carbon dono

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