Cas 1624286-11-8,(±)-2,8-dibromo-N-methyl-N-(p-tolyl)-6,12-dihydro-5,11-methanodibenzo[b,f][1,5]diazocin-13-amine

1624286-11-8

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Basic information

Product Name: (±)-2,8-dibromo-N-methyl-N-(p-tolyl)-6,12-dihydro-5,11-methanodibenzo[b,f][1,5]diazocin-13-amine
Synonyms: (±)-2,8-dibromo-N-methyl-N-(p-tolyl)-6,12-dihydro-5,11-methanodibenzo[b,f][1,5]diazocin-13-amine
CAS NO:1624286-11-8
Molecular Formula:
Molecular Weight: 499.248
EINECS: N/A
Product Categories: N/A
Mol File: 1624286-11-8.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: (±)-2,8-dibromo-N-methyl-N-(p-tolyl)-6,12-dihydro-5,11-methanodibenzo[b,f][1,5]diazocin-13-amine(CAS DataBase Reference)
NIST Chemistry Reference: (±)-2,8-dibromo-N-methyl-N-(p-tolyl)-6,12-dihydro-5,11-methanodibenzo[b,f][1,5]diazocin-13-amine(1624286-11-8)
EPA Substance Registry System: (±)-2,8-dibromo-N-methyl-N-(p-tolyl)-6,12-dihydro-5,11-methanodibenzo[b,f][1,5]diazocin-13-amine(1624286-11-8)

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: 1624286-11-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1624286-11-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,2,4,2,8 and 6 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1624286-11:
(9*1)+(8*6)+(7*2)+(6*4)+(5*2)+(4*8)+(3*6)+(2*1)+(1*1)=158
158 % 10 = 8
So 1624286-11-8 is a valid CAS Registry Number.

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1624286-11-8Relevant articles and documents

Discovery of Tro?ger's base analogues as selective inhibitors against human breast cancer cell line: Design, synthesis and cytotoxic evaluation

Manda, Bhaskar Reddy,Alla, Manjula,Ganji, Roopa Jones,Addlagatta, Anthony

, p. 39 - 47 (2014)

A library of structurally diverse Tr?ger's base analogues has been constructed via unusual amination of methylene bridge employing Vilsmeier-Haack conditions as well as by the incorporation of five and six membered heterocycles on the aromatic core of Tr?

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