Cas 75851-85-3,(5aS,5bR,8aS,8bS)-7-Benzyl-5-methyl-5a,5b,8a,8b-tetrahydro-4,7,10c-triaza-pentaleno[1,2,3-cd]phenalene-6,8-dione

75851-85-3

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Basic information

Product Name: (5aS,5bR,8aS,8bS)-7-Benzyl-5-methyl-5a,5b,8a,8b-tetrahydro-4,7,10c-triaza-pentaleno[1,2,3-cd]phenalene-6,8-dione
Synonyms: (5aS,5bR,8aS,8bS)-7-Benzyl-5-methyl-5a,5b,8a,8b-tetrahydro-4,7,10c-triaza-pentaleno[1,2,3-cd]phenalene-6,8-dione
CAS NO:75851-85-3
Molecular Formula:
Molecular Weight: 369.423
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: (5aS,5bR,8aS,8bS)-7-Benzyl-5-methyl-5a,5b,8a,8b-tetrahydro-4,7,10c-triaza-pentaleno[1,2,3-cd]phenalene-6,8-dione(CAS DataBase Reference)
NIST Chemistry Reference: (5aS,5bR,8aS,8bS)-7-Benzyl-5-methyl-5a,5b,8a,8b-tetrahydro-4,7,10c-triaza-pentaleno[1,2,3-cd]phenalene-6,8-dione(75851-85-3)
EPA Substance Registry System: (5aS,5bR,8aS,8bS)-7-Benzyl-5-methyl-5a,5b,8a,8b-tetrahydro-4,7,10c-triaza-pentaleno[1,2,3-cd]phenalene-6,8-dione(75851-85-3)

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: 75851-85-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 75851-85-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,8,5 and 1 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 75851-85:
(7*7)+(6*5)+(5*8)+(4*5)+(3*1)+(2*8)+(1*5)=163
163 % 10 = 3
So 75851-85-3 is a valid CAS Registry Number.

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75851-85-3Relevant academic research and scientific papers

CYCLOADDITION REACTION OF A NEW PERIPHERAL AZOMETHINE YLID TO SYMMETRICALLY SUBSTITUTED OLEFIN

Kanemasa, Shuji,Koira, Seigo,Kajigaeshi, Shoji

, p. 951 - 954 (2007/10/02)

An unusual azomethine ylid 1,3-dipole was generated on the periphery of pyridoquinoxaline ring.This peripheral ylid, anhydro 3H-pyridoquinoxalinium hydroxide, reacted stereoselectively with electron-deficient cis olefins such as dimeth

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