Cas 1064664-29-4,((E)-(3S,4S)-4-Benzyloxy-3-cyclohexyl-4-phenyl-but-1-enyl)-(4-methoxy-phenyl)-carbamic acid tert-butyl ester

1064664-29-4

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Basic information

Product Name: ((E)-(3S,4S)-4-Benzyloxy-3-cyclohexyl-4-phenyl-but-1-enyl)-(4-methoxy-phenyl)-carbamic acid tert-butyl ester
Synonyms: ((E)-(3S,4S)-4-Benzyloxy-3-cyclohexyl-4-phenyl-but-1-enyl)-(4-methoxy-phenyl)-carbamic acid tert-butyl ester
CAS NO:1064664-29-4
Molecular Formula:
Molecular Weight: 541.731
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: ((E)-(3S,4S)-4-Benzyloxy-3-cyclohexyl-4-phenyl-but-1-enyl)-(4-methoxy-phenyl)-carbamic acid tert-butyl ester(CAS DataBase Reference)
NIST Chemistry Reference: ((E)-(3S,4S)-4-Benzyloxy-3-cyclohexyl-4-phenyl-but-1-enyl)-(4-methoxy-phenyl)-carbamic acid tert-butyl ester(1064664-29-4)
EPA Substance Registry System: ((E)-(3S,4S)-4-Benzyloxy-3-cyclohexyl-4-phenyl-but-1-enyl)-(4-methoxy-phenyl)-carbamic acid tert-butyl ester(1064664-29-4)

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: 1064664-29-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1064664-29-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,6,4,6,6 and 4 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1064664-29:
(9*1)+(8*0)+(7*6)+(6*4)+(5*6)+(4*6)+(3*4)+(2*2)+(1*9)=154
154 % 10 = 4
So 1064664-29-4 is a valid CAS Registry Number.

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1064664-29-4Relevant academic research and scientific papers

Highly enantioselective syntheses of anti homoaldol products by (-)-sparteine-mediated lithiation/transmetalation/substitution of N-Boc allylic amines

Whisler, Marna C.,Vaillancourt, Louis,Beak, Peter

, p. 2655 - 2658 (2007/10/03)

(equation presented) (-)-Sparteine-mediated lithiation/transmetalation/substitution of N-Boc allylic amines provides anfi-configured homoaldol precursors in yields of 38-85% and enantiomeric ratios of 83:17-99:1. Subsequent O-protection and hydrolysis all

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