Cas 495402-84-1,2-(2,6-dichlorophenyl)-9-phenyltetrahydro-5H-pyrazolo[1,2-a]pyrrolo[3,4-c]pyrazole-1,3(2H,3aH)-dione

495402-84-1

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Basic information

Product Name: 2-(2,6-dichlorophenyl)-9-phenyltetrahydro-5H-pyrazolo[1,2-a]pyrrolo[3,4-c]pyrazole-1,3(2H,3aH)-dione
Synonyms: 2-(2,6-dichlorophenyl)-9-phenyltetrahydro-5H-pyrazolo[1,2-a]pyrrolo[3,4-c]pyrazole-1,3(2H,3aH)-dione
CAS NO:495402-84-1
Molecular Formula: C20H17Cl2N3O2
Molecular Weight: 402.27388
EINECS: N/A
Product Categories: N/A
Mol File: 495402-84-1.mol

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: /
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 2-(2,6-dichlorophenyl)-9-phenyltetrahydro-5H-pyrazolo[1,2-a]pyrrolo[3,4-c]pyrazole-1,3(2H,3aH)-dione(CAS DataBase Reference)
NIST Chemistry Reference: 2-(2,6-dichlorophenyl)-9-phenyltetrahydro-5H-pyrazolo[1,2-a]pyrrolo[3,4-c]pyrazole-1,3(2H,3aH)-dione(495402-84-1)
EPA Substance Registry System: 2-(2,6-dichlorophenyl)-9-phenyltetrahydro-5H-pyrazolo[1,2-a]pyrrolo[3,4-c]pyrazole-1,3(2H,3aH)-dione(495402-84-1)

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: 495402-84-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 495402-84-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,9,5,4,0 and 2 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 495402-84:
(8*4)+(7*9)+(6*5)+(5*4)+(4*0)+(3*2)+(2*8)+(1*4)=171
171 % 10 = 1
So 495402-84-1 is a valid CAS Registry Number.

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495402-84-1Relevant academic research and scientific papers

Stereoselectivity in the addition of 1,3-dipolarophiles to 6-aryl-1,5-diazabicyclo[3.1.0]hexanes

Molchanov,Sipkin,Koptelov,Kopf,Kostikov

, p. 1338 - 1345 (2007/10/03)

Thermolysis of 6-aryl-1,5-diazabicyclo[3.1.0]hexanes in the presence of N-arylmaleimides having a substituent in the ortho position of the aromatic ring leads to predominant formation of the corresponding trans-9- arylperhydropyrazolo[1,2-a]pyrrolo[3,4-c]

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