Cas 86926-91-2,Phenyl-(2,4,6a-triphenyl-4a,6a-dihydro-1-thia-3,6b-diaza-cyclopenta[cd]pentalen-6-yl)-methanone

86926-91-2

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Basic information

Product Name: Phenyl-(2,4,6a-triphenyl-4a,6a-dihydro-1-thia-3,6b-diaza-cyclopenta[cd]pentalen-6-yl)-methanone
Synonyms: Phenyl-(2,4,6a-triphenyl-4a,6a-dihydro-1-thia-3,6b-diaza-cyclopenta[cd]pentalen-6-yl)-methanone
CAS NO:86926-91-2
Molecular Formula:
Molecular Weight: 482.605
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: Phenyl-(2,4,6a-triphenyl-4a,6a-dihydro-1-thia-3,6b-diaza-cyclopenta[cd]pentalen-6-yl)-methanone(CAS DataBase Reference)
NIST Chemistry Reference: Phenyl-(2,4,6a-triphenyl-4a,6a-dihydro-1-thia-3,6b-diaza-cyclopenta[cd]pentalen-6-yl)-methanone(86926-91-2)
EPA Substance Registry System: Phenyl-(2,4,6a-triphenyl-4a,6a-dihydro-1-thia-3,6b-diaza-cyclopenta[cd]pentalen-6-yl)-methanone(86926-91-2)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 86926-91-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 86926-91-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,9,2 and 6 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 86926-91:
(7*8)+(6*6)+(5*9)+(4*2)+(3*6)+(2*9)+(1*1)=182
182 % 10 = 2
So 86926-91-2 is a valid CAS Registry Number.

86926-91-2Upstream product

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86926-91-2Relevant academic research and scientific papers

CYCLOADDITION REACTION OF IMIDAZOTHIAIVZOLE TO ACETYLENIC DIPOLAROPHILES AND NOVEL CONVERSION OF CYCLOADDUCTS INTO 4,9c-DIAZAPENTALENONAPHTHALENES

Tsuge, Otohiko,Kanemasa, Shuji,Hamamoto, Takayoshi

, p. 763 - 766 (2007/10/02)

A nitrogen-bridged tetravalent sulfur compound, 1,3,6-triphenylimidazothiaIVzole, reacts with several acetylenic dipolarophiles giving excellent yields of regio- and periselective cycloadducts to the azomethine ylide 1,3-dipole of

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