Cas 76900-48-6,5,6,14,15,20,21-Hexaphenylheptacyclo<8.8.4.13,17.18,12.04,7.013,16.019,22>tetracosa-1,3(23),8,10,12(24),17-hexaen

76900-48-6

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Basic information

Product Name: 5,6,14,15,20,21-Hexaphenylheptacyclo<8.8.4.1^3,17.1^8,12.0^4,7.0^13,16.0^19,22>tetracosa-1,3(23),8,10,12(24),17-hexaen
Synonyms:
CAS NO:76900-48-6
Molecular Formula:
Molecular Weight: 769.041
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: 5,6,14,15,20,21-Hexaphenylheptacyclo<8.8.4.1^3,17.1^8,12.0^4,7.0^13,16.0^19,22>tetracosa-1,3(23),8,10,12(24),17-hexaen(CAS DataBase Reference)
NIST Chemistry Reference: 5,6,14,15,20,21-Hexaphenylheptacyclo<8.8.4.1^3,17.1^8,12.0^4,7.0^13,16.0^19,22>tetracosa-1,3(23),8,10,12(24),17-hexaen(76900-48-6)
EPA Substance Registry System: 5,6,14,15,20,21-Hexaphenylheptacyclo<8.8.4.1^3,17.1^8,12.0^4,7.0^13,16.0^19,22>tetracosa-1,3(23),8,10,12(24),17-hexaen(76900-48-6)

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: 76900-48-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 76900-48-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,9,0 and 0 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 76900-48:
(7*7)+(6*6)+(5*9)+(4*0)+(3*0)+(2*4)+(1*8)=146
146 % 10 = 6
So 76900-48-6 is a valid CAS Registry Number.

76900-48-6Upstream product

34631-15-7 (E)-1,3,5-tri((E)-styryl)benzene

76900-48-6Downstream Products

76900-48-6Relevant academic research and scientific papers

Photochemistry of 1,3,5-Tristyrylbenzene

Winter, Werner,Langjahr, Ursula,Meier, Herbert,Merkuschew, Jewgeni,Juriew, Juri

, p. 2452 - 2463 (2007/10/02)

Depending on the reaction conditions the irradiation of the title compound 1 yields the cyclophane 5, the pyrene derivative 6, or the polycondensed aromatic system 9.An X-ray analysis was performed for 5, representing a new type of cyclophane in which two benzene rings are bridged again by rings.

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