Cas 491838-94-9,4H-1,2-Oxazine, 5-butyl-5,6-dihydro-6-[[(1R,2S,5R)-5-methyl-2-(1-methylethyl)cyclohexyl] oxy]-3-phenyl-, (5S,6S)-

491838-94-9

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Basic information

Product Name: 4H-1,2-Oxazine, 5-butyl-5,6-dihydro-6-[[(1R,2S,5R)-5-methyl-2-(1-methylethyl)cyclohexyl] oxy]-3-phenyl-, (5S,6S)-
Synonyms:
CAS NO:491838-94-9
Molecular Formula: C24H37NO2
Molecular Weight: 371.563
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: 4H-1,2-Oxazine, 5-butyl-5,6-dihydro-6-[[(1R,2S,5R)-5-methyl-2-(1-methylethyl)cyclohexyl] oxy]-3-phenyl-, (5S,6S)-(CAS DataBase Reference)
NIST Chemistry Reference: 4H-1,2-Oxazine, 5-butyl-5,6-dihydro-6-[[(1R,2S,5R)-5-methyl-2-(1-methylethyl)cyclohexyl] oxy]-3-phenyl-, (5S,6S)-(491838-94-9)
EPA Substance Registry System: 4H-1,2-Oxazine, 5-butyl-5,6-dihydro-6-[[(1R,2S,5R)-5-methyl-2-(1-methylethyl)cyclohexyl] oxy]-3-phenyl-, (5S,6S)-(491838-94-9)

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: 491838-94-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 491838-94-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,9,1,8,3 and 8 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 491838-94:
(8*4)+(7*9)+(6*1)+(5*8)+(4*3)+(3*8)+(2*9)+(1*4)=199
199 % 10 = 9
So 491838-94-9 is a valid CAS Registry Number.

491838-94-9Upstream product

491838-94-9Downstream Products

491838-94-9Relevant academic research and scientific papers

Synthesis of enantioenriched 2-substituted 4-phenylbutylamines by hydrogenolysis of optically pure 6-alkoxy-5,6-dihydro-4H-1,2-oxazines

Buchholz, Monika,Hiller, Florian,Reissig, Hans-Ulrich

, p. 2838 - 2843 (2007/10/03)

Lewis acid promoted exchange of the 6-ethoxy group of 6H- 1,2-oxazines 1-3 with (-)-menthol furnished the optically active heterocycles 4-6. Diastereomers 4a and 4b, which could be separated efficiently by chromatography, were excellent substrates for hig

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