Cas 151474-89-4,14-amino-6a,13a-dimethyl-6,6a,13,13a-tetrahydroquino[3',2':4,5]pentaleno[2,1-b]quinolin-7-ylamine

151474-89-4

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Basic information

Product Name: 14-amino-6a,13a-dimethyl-6,6a,13,13a-tetrahydroquino[3',2':4,5]pentaleno[2,1-b]quinolin-7-ylamine
Synonyms: 14-amino-6a,13a-dimethyl-6,6a,13,13a-tetrahydroquino[3',2':4,5]pentaleno[2,1-b]quinolin-7-ylamine
CAS NO:151474-89-4
Molecular Formula: C24H22N4
Molecular Weight: 366.45828
EINECS: N/A
Product Categories: N/A
Mol File: 151474-89-4.mol

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: /
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 14-amino-6a,13a-dimethyl-6,6a,13,13a-tetrahydroquino[3',2':4,5]pentaleno[2,1-b]quinolin-7-ylamine(CAS DataBase Reference)
NIST Chemistry Reference: 14-amino-6a,13a-dimethyl-6,6a,13,13a-tetrahydroquino[3',2':4,5]pentaleno[2,1-b]quinolin-7-ylamine(151474-89-4)
EPA Substance Registry System: 14-amino-6a,13a-dimethyl-6,6a,13,13a-tetrahydroquino[3',2':4,5]pentaleno[2,1-b]quinolin-7-ylamine(151474-89-4)

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: 151474-89-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 151474-89-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,1,4,7 and 4 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 151474-89:
(8*1)+(7*5)+(6*1)+(5*4)+(4*7)+(3*4)+(2*8)+(1*9)=134
134 % 10 = 4
So 151474-89-4 is a valid CAS Registry Number.

151474-89-4Upstream product

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151474-89-4Relevant academic research and scientific papers

Synthesis and evaluation of tacrine-related compounds for the treatment of Alzheimer's disease

Aguado, F.,Badia, A.,Banos, J.E.,Bosch, F.,Bozzo, C.,et al.

, p. 205 - 222 (2007/10/02)

A number of polycyclic compounds related to tacrine have been prepared by condensation of ortho-aminobenzonitriles and 2-aminocyclopentenecarbonitrile with several C2v-symmetric diketones under AlCl3 or ZnCl2 catalysis.Monocondensation products

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