Cas 862250-76-8,1-benzoyl-4,6-dibromo-3-methyl-1,4,5,6-tetrahydrocyclopenta[c]pyrazole

862250-76-8

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Basic information

Product Name: 1-benzoyl-4,6-dibromo-3-methyl-1,4,5,6-tetrahydrocyclopenta[c]pyrazole
Synonyms: 1-benzoyl-4,6-dibromo-3-methyl-1,4,5,6-tetrahydrocyclopenta[c]pyrazole
CAS NO:862250-76-8
Molecular Formula:
Molecular Weight: 384.07
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: 1-benzoyl-4,6-dibromo-3-methyl-1,4,5,6-tetrahydrocyclopenta[c]pyrazole(CAS DataBase Reference)
NIST Chemistry Reference: 1-benzoyl-4,6-dibromo-3-methyl-1,4,5,6-tetrahydrocyclopenta[c]pyrazole(862250-76-8)
EPA Substance Registry System: 1-benzoyl-4,6-dibromo-3-methyl-1,4,5,6-tetrahydrocyclopenta[c]pyrazole(862250-76-8)

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: 862250-76-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 862250-76-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,2,2,5 and 0 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 862250-76:
(8*8)+(7*6)+(6*2)+(5*2)+(4*5)+(3*0)+(2*7)+(1*6)=168
168 % 10 = 8
So 862250-76-8 is a valid CAS Registry Number.

862250-76-8Upstream product

546958-28-5 1-benzoyl-1,4,6,6-tetrahydro-3-methyl-cyclopenta[c]pyrazole

862250-76-8Downstream Products

862250-76-8Relevant academic research and scientific papers

Synthesis of polycyclic pyrazoles through formation of the first fused heterocyclic o-quinodimethane intermediate

Konstantinidou, Despina,Papageorgiou, Marina,Stephanidou-Stephanatou,Tsoleridis, Constantinos A.

, p. 4843 - 4845 (2005)

1-Benzoyl-4,6-dibromo-3-methyl-1,4,5,6-tetrahydrocyclopenta[c]pyrazole (2) was used as a precursor for o-quinodimethane 3, which was trapped by in situ reactions with dienophiles to give bridged pyrazole derivatives.

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