Cas 1347752-58-2,2,3,8,9,14,15-hexabenzyldiquinoxalino[2,3-a:2',3'-c]phenazine-2,3,8,9,14,15-hexaamine

1347752-58-2

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Basic information

Product Name: 2,3,8,9,14,15-hexabenzyldiquinoxalino[2,3-a:2',3'-c]phenazine-2,3,8,9,14,15-hexaamine
Synonyms: 2,3,8,9,14,15-hexabenzyldiquinoxalino[2,3-a:2',3'-c]phenazine-2,3,8,9,14,15-hexaamine
CAS NO:1347752-58-2
Molecular Formula:
Molecular Weight: 1015.24
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: 2,3,8,9,14,15-hexabenzyldiquinoxalino[2,3-a:2',3'-c]phenazine-2,3,8,9,14,15-hexaamine(CAS DataBase Reference)
NIST Chemistry Reference: 2,3,8,9,14,15-hexabenzyldiquinoxalino[2,3-a:2',3'-c]phenazine-2,3,8,9,14,15-hexaamine(1347752-58-2)
EPA Substance Registry System: 2,3,8,9,14,15-hexabenzyldiquinoxalino[2,3-a:2',3'-c]phenazine-2,3,8,9,14,15-hexaamine(1347752-58-2)

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: 1347752-58-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1347752-58-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,4,7,7,5 and 2 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1347752-58:
(9*1)+(8*3)+(7*4)+(6*7)+(5*7)+(4*5)+(3*2)+(2*5)+(1*8)=182
182 % 10 = 2
So 1347752-58-2 is a valid CAS Registry Number.

1347752-58-2Upstream product

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1347752-58-2Relevant academic research and scientific papers

Novel organogelators based on amine-derived hexaazatrinaphthylene

Velazquez, Daniel Garcia,Orive, Alejandro Gonzalez,Creus, Alberto Hernandez,Luque, Rafael,Ravelo, Angel Gutierrez

, p. 6524 - 6527 (2011)

Novel C3-symmetrical heteroaromatic hexaazatrinaphthylene (HATNA) gelators symmetrically end-substituted with pendant aromatic and aliphatic amines were synthesized. Some of these π-conjugated structures induce self-assembly, forming fibers abl

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