Cas 299908-88-6,(3R,4R)-N-(t-butoxycarbonyl)-N-(4-methoxyphenyl)-3-cyclohexyl-4-hydroxy-4-phenyl-(Z)-1-butene-1-amine

299908-88-6

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Basic information

Product Name: (3R,4R)-N-(t-butoxycarbonyl)-N-(4-methoxyphenyl)-3-cyclohexyl-4-hydroxy-4-phenyl-(Z)-1-butene-1-amine
Synonyms: (3R,4R)-N-(t-butoxycarbonyl)-N-(4-methoxyphenyl)-3-cyclohexyl-4-hydroxy-4-phenyl-(Z)-1-butene-1-amine
CAS NO:299908-88-6
Molecular Formula:
Molecular Weight: 451.606
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: (3R,4R)-N-(t-butoxycarbonyl)-N-(4-methoxyphenyl)-3-cyclohexyl-4-hydroxy-4-phenyl-(Z)-1-butene-1-amine(CAS DataBase Reference)
NIST Chemistry Reference: (3R,4R)-N-(t-butoxycarbonyl)-N-(4-methoxyphenyl)-3-cyclohexyl-4-hydroxy-4-phenyl-(Z)-1-butene-1-amine(299908-88-6)
EPA Substance Registry System: (3R,4R)-N-(t-butoxycarbonyl)-N-(4-methoxyphenyl)-3-cyclohexyl-4-hydroxy-4-phenyl-(Z)-1-butene-1-amine(299908-88-6)

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: 299908-88-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 299908-88-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,9,9,0 and 8 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 299908-88:
(8*2)+(7*9)+(6*9)+(5*9)+(4*0)+(3*8)+(2*8)+(1*8)=226
226 % 10 = 6
So 299908-88-6 is a valid CAS Registry Number.

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299908-88-6Relevant 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 (2000)

(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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