Cas 71709-05-2,2-<(benzyloxycarbonyl)(3,4-dimethoxyphenethyl)amino>-1-(4-benzyloxyphenyl)ethanone

71709-05-2

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Basic information

Product Name: 2-<(benzyloxycarbonyl)(3,4-dimethoxyphenethyl)amino>-1-(4-benzyloxyphenyl)ethanone
Synonyms: 2-<(benzyloxycarbonyl)(3,4-dimethoxyphenethyl)amino>-1-(4-benzyloxyphenyl)ethanone
CAS NO:71709-05-2
Molecular Formula:
Molecular Weight: 539.628
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: 2-<(benzyloxycarbonyl)(3,4-dimethoxyphenethyl)amino>-1-(4-benzyloxyphenyl)ethanone(CAS DataBase Reference)
NIST Chemistry Reference: 2-<(benzyloxycarbonyl)(3,4-dimethoxyphenethyl)amino>-1-(4-benzyloxyphenyl)ethanone(71709-05-2)
EPA Substance Registry System: 2-<(benzyloxycarbonyl)(3,4-dimethoxyphenethyl)amino>-1-(4-benzyloxyphenyl)ethanone(71709-05-2)

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: 71709-05-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 71709-05-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,7,0 and 9 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 71709-05:
(7*7)+(6*1)+(5*7)+(4*0)+(3*9)+(2*0)+(1*5)=122
122 % 10 = 2
So 71709-05-2 is a valid CAS Registry Number.

71709-05-2Upstream product

501-53-1 benzyl chloroformate

71709-05-2Downstream Products

71709-05-2Relevant academic research and scientific papers

Asymmetric reduction of aromatic ketones. I. Enantioselective synthesis of denopamine

Kawaguchi,Saito,Matsuki,Iwakuma,Takeda

, p. 639 - 642 (2007/10/02)

Asymmetric reduction of the N-protected amino ketone (2) with several chiral reducing agents, i.e., (R)-(+)-2-amino-3-methyl-1,1-diphenylbutanol (6)-borane complex (method A), (S,S')-N,N'-dibenzoylcystine (7)-LiBH4-ROH complex (method B), and s

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