Cas 6150-02-3,(α<sup>1</sup>S)-α-phenyl-1-naphthalenemethanamine

6150-02-3

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Basic information

Product Name: (α¹S)-α-phenyl-1-naphthalenemethanamine
Synonyms:
CAS NO:6150-02-3
Molecular Formula:
Molecular Weight: 233.313
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: (α¹S)-α-phenyl-1-naphthalenemethanamine(CAS DataBase Reference)
NIST Chemistry Reference: (α¹S)-α-phenyl-1-naphthalenemethanamine(6150-02-3)
EPA Substance Registry System: (α¹S)-α-phenyl-1-naphthalenemethanamine(6150-02-3)

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: 6150-02-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 6150-02-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,5 and 0 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6150-02:
(6*6)+(5*1)+(4*5)+(3*0)+(2*0)+(1*2)=63
63 % 10 = 3
So 6150-02-3 is a valid CAS Registry Number.

6150-02-3Upstream product

6150-02-3Downstream Products

102559-35-3 (R)-3,5-dihydroxy-3-methyl-valeric acid-[((S)-[1]naphthyl-phenyl-methyl)-amide]

6150-02-3Relevant academic research and scientific papers

Asymmetric Induction in the Reduction of Optically Active N-Alkylidenesulphinamides by Metal Hydrides. A New, Efficient Enantioselective Route to Chiral Amines

Annunziata, Rita,Cinquini, Mauro,Cozzi, Franco

, p. 339 - 344 (2007/10/02)

A series of racemic and optically active N-alkylidenesulphinamides has been prepared and their reduction by metal hydrides studied.The extent of asymmetric synthesis mainly depends on the nature of the reducing species; the best results (up to 92percent of stereoselectivity) are obtained with alkoxy-lithium aluminium hydrides.A new, highly enantioselective synthesis of amines is described.

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