Cas 123676-18-6,12-(p-nitrobenzoyl)-1,3-dichloro-6,11-diphenyl-11,12-dihydro-6,11<1',2'>-benzeno-6H-dibenz<b,f><1,4>oxazocine

123676-18-6

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Basic information

Product Name: 12-(p-nitrobenzoyl)-1,3-dichloro-6,11-diphenyl-11,12-dihydro-6,11<1',2'>-benzeno-6H-dibenz<1,4>oxazocine
Synonyms:
CAS NO:123676-18-6
Molecular Formula:
Molecular Weight: 655.537
EINECS: N/A
Product Categories: N/A
Mol File: 123676-18-6.mol
Article Data: 1

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: 12-(p-nitrobenzoyl)-1,3-dichloro-6,11-diphenyl-11,12-dihydro-6,11<1',2'>-benzeno-6H-dibenz<1,4>oxazocine(CAS DataBase Reference)
NIST Chemistry Reference: 12-(p-nitrobenzoyl)-1,3-dichloro-6,11-diphenyl-11,12-dihydro-6,11<1',2'>-benzeno-6H-dibenz<1,4>oxazocine(123676-18-6)
EPA Substance Registry System: 12-(p-nitrobenzoyl)-1,3-dichloro-6,11-diphenyl-11,12-dihydro-6,11<1',2'>-benzeno-6H-dibenz<1,4>oxazocine(123676-18-6)

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: 123676-18-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 123676-18-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,3,6,7 and 6 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 123676-18:
(8*1)+(7*2)+(6*3)+(5*6)+(4*7)+(3*6)+(2*1)+(1*8)=126
126 % 10 = 6
So 123676-18-6 is a valid CAS Registry Number.

123676-18-6Upstream product

123676-18-6Downstream Products

123676-18-6Relevant articles and documents

Reactions of an o-Quinone Monoimide with Anthracenes, Phencyclone, and 1,3-Diphenylisobenzofuran

Heine, Harold W.,Suriano, Joseph A.,Winkel, Chris,Burik, Andrea,Taylor, Carol M.

, p. 5926 - 5930 (2007/10/02)

The o-quinone monoimide N-(2,4-dichloro-6-oxo-2,4-cyclohexadien-1-ylidene)-4-nitrobenzamide (1) reacts at ambient temperature and in the absence of light with anthracene, 9-substituted anthracenes, and 9,10-diphenylanthracene to give the 4? + 4? cycloaddu

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