Cas 1357289-76-9,(+/-)-2,8-dimethoxy-N,2,8-trimethyl-N-(p-tolyl)-6H,12H-5,11-methanodibenzo[b,f][1,5]diazocin-13-amine

1357289-76-9

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Basic information

Product Name: (+/-)-2,8-dimethoxy-N,2,8-trimethyl-N-(p-tolyl)-6H,12H-5,11-methanodibenzo[b,f][1,5]diazocin-13-amine
Synonyms: (+/-)-2,8-dimethoxy-N,2,8-trimethyl-N-(p-tolyl)-6H,12H-5,11-methanodibenzo[b,f][1,5]diazocin-13-amine
CAS NO:1357289-76-9
Molecular Formula:
Molecular Weight: 401.508
EINECS: N/A
Product Categories: N/A
Mol File: 1357289-76-9.mol
Article Data: 2

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-dimethoxy-N,2,8-trimethyl-N-(p-tolyl)-6H,12H-5,11-methanodibenzo[b,f][1,5]diazocin-13-amine(CAS DataBase Reference)
NIST Chemistry Reference: (+/-)-2,8-dimethoxy-N,2,8-trimethyl-N-(p-tolyl)-6H,12H-5,11-methanodibenzo[b,f][1,5]diazocin-13-amine(1357289-76-9)
EPA Substance Registry System: (+/-)-2,8-dimethoxy-N,2,8-trimethyl-N-(p-tolyl)-6H,12H-5,11-methanodibenzo[b,f][1,5]diazocin-13-amine(1357289-76-9)

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: 1357289-76-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1357289-76-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,7,2,8 and 9 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1357289-76:
(9*1)+(8*3)+(7*5)+(6*7)+(5*2)+(4*8)+(3*9)+(2*7)+(1*6)=199
199 % 10 = 9
So 1357289-76-9 is a valid CAS Registry Number.

1357289-76-9Upstream product

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1357289-76-9Relevant articles and documents

Regioselective synthesis of dimethylamino- or arylalkylamino- "crowned" troeger's base analogues under Vilsmeier-Haack conditions

Reddy, Manda Bhaskar,Manjula, Alla,Rao, Bommena Vittal,Sridhar, Balasubramanian

, p. 312 - 319 (2012)

Under typical Vilsmeier-Haack conditions, Troeger's base undergoes regioselective dimethylamino or arylalkylamino substitution on the methano bridge of the dibenzo[b,f][1,5]diazocine system, revealing a hitherto unknown reactivity pattern. The regioselect

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