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3-phenylcyclohepta[4,5]pyrrolo[1,2-a]-1,3,5-triazine-2,4(3H)-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

182485-60-5

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182485-60-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 182485-60-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,2,4,8 and 5 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 182485-60:
(8*1)+(7*8)+(6*2)+(5*4)+(4*8)+(3*5)+(2*6)+(1*0)=155
155 % 10 = 5
So 182485-60-5 is a valid CAS Registry Number.

182485-60-5Downstream Products

182485-60-5Relevant academic research and scientific papers

Reactions of 2-triphenylphosphoimino-1-azaazulenes with aryl isocyanates and aryl isothiocyanates

Nagamatsu, Kentaro,Serita, Ai,Zeng, Jun-Hau,Fujii, Hiroyuki,Abe, Noritaka,Kakehi, Akikazu

, p. 337 - 351 (2007/10/03)

Reaction of 2-triphenylphosphoimino-1-azaazulenes (4a-c), prepared from 2-amino-1-azaazulenes, with some aryl isocyanates gave 2-arylimino-3-aryl-2,3,4,4a-tetrahydro-1,3,4a-triazabenz[a]azulen-4-one (6) as major products. Reaction of aryl isothiocyanates

Synthesis and properties of 3-arylcyclohepta[4,5]-pyrrolo[1,2-a]-1,3,5-triazine-2,4(3H)-diones and related compounds: Photo-induced autorecycling oxidation of amines

Nitta, Makoto,Morito, Tomoyuki,Mitsumoto, Yuhki,Naya, Shin-ichi

, p. 1629 - 1639 (2007/10/03)

3-Phenyl- and 3-(4-nitrophenyl)cyclohepta[4,5]pyrrolo[1,2-a]-1,3,5-triazine-2,4(3H)-diones and the corresponding arylimino derivatives (5a,b) and (6a,b) were synthesized by the reaction of (1-azaazulen-2-yl)iminotriphenylphosphorane with aryl isocyanates

Reactions of 2-amino-, 2-alkylamino-, and 2-piperidino-1-azaazulenes with aryl and chlorosulfonyl isocyanates

Abe, Noritaka,Matsuda, Haruhiko,Sugihara, Yoshikazu,Kakehi, Akikazu

, p. 1323 - 1331 (2007/10/03)

Reaction of 2-amino-1-azaazulene with phenyl isocyanate gave 3-phenyl-2H-3,4-dihydro-1,3,4a-triazabenz[5,4-a]azulene-2,4-dione. Reactions of 2-alkylamino-1-azaazulenes with aryl isocyanates gave 2-(N-ethyl-N-arylureido)-1-azaazulenes initially, which rearranged to N-aryl-2-alkylamino-1-azaazulene-3-carboxamides and successive reaction with another molar amount of aryl isocyanate furnished uracil-fuzed 1-azaazulenes. Reaction of 2-piperidino-1-azaazulene with aryl isocyanate gave N-aryl-2-piperidino-1-azaazulene-3-carboxamide. Reaction of 2-(substituted amino)-1-azaazulenes with chlorosulfonyl isocyanate gave 3-cyano- and 3-chloro-2-(substituted amino)-1-azaazulenes.

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