Cas 329969-52-0,(4-Methoxy-phenyl)-((Z)-(3S,4S)-6-methyl-4-nitromethyl-3-phenyl-hept-1-enyl)-carbamic acid tert-butyl ester

329969-52-0

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Basic information

Product Name: (4-Methoxy-phenyl)-((Z)-(3S,4S)-6-methyl-4-nitromethyl-3-phenyl-hept-1-enyl)-carbamic acid tert-butyl ester
Synonyms: (4-Methoxy-phenyl)-((Z)-(3S,4S)-6-methyl-4-nitromethyl-3-phenyl-hept-1-enyl)-carbamic acid tert-butyl ester
CAS NO:329969-52-0
Molecular Formula:
Molecular Weight: 468.593
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: (4-Methoxy-phenyl)-((Z)-(3S,4S)-6-methyl-4-nitromethyl-3-phenyl-hept-1-enyl)-carbamic acid tert-butyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (4-Methoxy-phenyl)-((Z)-(3S,4S)-6-methyl-4-nitromethyl-3-phenyl-hept-1-enyl)-carbamic acid tert-butyl ester(329969-52-0)
EPA Substance Registry System: (4-Methoxy-phenyl)-((Z)-(3S,4S)-6-methyl-4-nitromethyl-3-phenyl-hept-1-enyl)-carbamic acid tert-butyl ester(329969-52-0)

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: 329969-52-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 329969-52-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,9,9,6 and 9 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 329969-52:
(8*3)+(7*2)+(6*9)+(5*9)+(4*6)+(3*9)+(2*5)+(1*2)=200
200 % 10 = 0
So 329969-52-0 is a valid CAS Registry Number.

329969-52-0Upstream product

34209-90-0 (E)-4-methyl-1-nitro-1-pentene

329969-52-0Downstream Products

329969-59-7 (4R,5S)-5-isobutyl-4-phenyl-piperidin-2-one

329969-52-0Relevant academic research and scientific papers

Asymmetric carbon-carbon bond formations in conjugate additions of lithiated N-Boc allylic and benzylic amines to nitroalkenes: Enantioselective synthesis of substituted piperidines, pyrrolidines, and pyrimidinones

Johnson, Timothy A.,Jang, Doo Ok,Slafer, Brian W.,Curtis, Michael D.,Beak, Peter

, p. 11689 - 11698 (2007/10/03)

(-)-Sparteine mediated lithiations of N-Boc-allylic and benzylic amines provide configurationally stable intermediates which on conjugate additions to nitroalkenes provide highly enantioenriched enecarbamate products in good yields, and with high diastere

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