Cas 794469-18-4,(M,R)-1-(2-methoxy-4,6-dimethylphenyl)-2-[N-methyl-N-(1-phenylethyl)aminomethyl]naphthalene

794469-18-4

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Basic information

Product Name: (M,R)-1-(2-methoxy-4,6-dimethylphenyl)-2-[N-methyl-N-(1-phenylethyl)aminomethyl]naphthalene
Synonyms:
CAS NO:794469-18-4
Molecular Formula:
Molecular Weight: 409.571
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: (M,R)-1-(2-methoxy-4,6-dimethylphenyl)-2-[N-methyl-N-(1-phenylethyl)aminomethyl]naphthalene(CAS DataBase Reference)
NIST Chemistry Reference: (M,R)-1-(2-methoxy-4,6-dimethylphenyl)-2-[N-methyl-N-(1-phenylethyl)aminomethyl]naphthalene(794469-18-4)
EPA Substance Registry System: (M,R)-1-(2-methoxy-4,6-dimethylphenyl)-2-[N-methyl-N-(1-phenylethyl)aminomethyl]naphthalene(794469-18-4)

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: 794469-18-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 794469-18-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,9,4,4,6 and 9 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 794469-18:
(8*7)+(7*9)+(6*4)+(5*4)+(4*6)+(3*9)+(2*1)+(1*8)=224
224 % 10 = 4
So 794469-18-4 is a valid CAS Registry Number.

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794469-18-4Relevant academic research and scientific papers

Synthesis and antitrypanosomal activity of 2-aminomethyl-1-(2-oxyphenyl) naphthalenes

Bringmann, Gerhard,Pfeifer, Robert-Michael,Schreiber, Petra,Hartner, Kristina,Kocher, Nikolaus,Brun, Reto,Peters, Karl,Peters, Eva-Maria,Breuning, Matthias

, p. 6335 - 6344 (2007/10/03)

A broad variety of enantiopure axially chiral 2-aminomethyl-1-(2-oxyphenyl) naphthalenes were prepared via short and efficient synthetic pathways by using the 'lactone method' for the regio- and stereoselective construction of the biaryl axis. Their in vi

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