Cas 51474-82-9,2-phenyl-tetrahydro-5r,10c-ethano-5ac,9ac-[2]oxapropano-[1,2,4]triazolo[1,2-b]phthalazine-1,3-dione

51474-82-9

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Basic information

Product Name: 2-phenyl-tetrahydro-5r,10c-ethano-5ac,9ac-[2]oxapropano-[1,2,4]triazolo[1,2-b]phthalazine-1,3-dione
Synonyms:
CAS NO:51474-82-9
Molecular Formula:
Molecular Weight: 353.421
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: 2-phenyl-tetrahydro-5r,10c-ethano-5ac,9ac-[2]oxapropano-[1,2,4]triazolo[1,2-b]phthalazine-1,3-dione(CAS DataBase Reference)
NIST Chemistry Reference: 2-phenyl-tetrahydro-5r,10c-ethano-5ac,9ac-[2]oxapropano-[1,2,4]triazolo[1,2-b]phthalazine-1,3-dione(51474-82-9)
EPA Substance Registry System: 2-phenyl-tetrahydro-5r,10c-ethano-5ac,9ac-[2]oxapropano-[1,2,4]triazolo[1,2-b]phthalazine-1,3-dione(51474-82-9)

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: 51474-82-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 51474-82-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,4,7 and 4 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 51474-82:
(7*5)+(6*1)+(5*4)+(4*7)+(3*4)+(2*8)+(1*2)=119
119 % 10 = 9
So 51474-82-9 is a valid CAS Registry Number.

51474-82-9Upstream product

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51474-82-9Relevant academic research and scientific papers

Propellanes-XXVII. Reactions of 4-phenyl-1,2,4-triazoline-3,5-dione with some [4.4.3]propellane ethers, imides and their irontricarbonyl derivatives

Amith,Ginsburg

, p. 3415 - 3422 (1974)

The steric course of Diels-Alder reactions of propellane ethers and methylimides, at different oxidation levels, was investigated. Irontricarbonyl derivatives, particularly of the imides, were subjected to reaction with a potent dienophile and the results

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