Cas 128113-65-5,(1S,1'S)-N-(1'-phenylethyl)-1-(2''-isopropoxy-3'',4''-dimethoxyphenyl)ethylamine hydrobromide

128113-65-5

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Basic information

Product Name: (1S,1'S)-N-(1'-phenylethyl)-1-(2''-isopropoxy-3'',4''-dimethoxyphenyl)ethylamine hydrobromide
Synonyms: (1S,1'S)-N-(1'-phenylethyl)-1-(2''-isopropoxy-3'',4''-dimethoxyphenyl)ethylamine hydrobromide
CAS NO:128113-65-5
Molecular Formula:
Molecular Weight: 424.378
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: (1S,1'S)-N-(1'-phenylethyl)-1-(2''-isopropoxy-3'',4''-dimethoxyphenyl)ethylamine hydrobromide(CAS DataBase Reference)
NIST Chemistry Reference: (1S,1'S)-N-(1'-phenylethyl)-1-(2''-isopropoxy-3'',4''-dimethoxyphenyl)ethylamine hydrobromide(128113-65-5)
EPA Substance Registry System: (1S,1'S)-N-(1'-phenylethyl)-1-(2''-isopropoxy-3'',4''-dimethoxyphenyl)ethylamine hydrobromide(128113-65-5)

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: 128113-65-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 128113-65-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,1,1 and 3 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 128113-65:
(8*1)+(7*2)+(6*8)+(5*1)+(4*1)+(3*3)+(2*6)+(1*5)=105
105 % 10 = 5
So 128113-65-5 is a valid CAS Registry Number.

128113-65-5Upstream product

128113-65-5Downstream Products

128113-86-0 (S)-1-(2'-isopropoxy-3',4'-dimethoxyphenyl)ethylamine hydrobromide

128113-65-5Relevant academic research and scientific papers

ENANTIOMERICALLY PURE OXYGENATED 1-PHENYLETHYLAMINES FROM SUBSTITUTED ACETOPHENONES: BY REDUCTIVE AMINATION AND REGIOSPECIFIC CLEAVAGE

Bringmann, Gerhard,Geisler, Joerg-Peter

, p. 317 - 320 (2007/10/02)

An efficient method for the asymmetric synthesis of chiral, oxygenated 1-phenylethylamines (1) in essentially two steps is described.The substituted acetophenones 2 are reductively aminated with unsubstituted chiral 1-phenylethylamine ("PEA",3), via the c

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