Cas 956350-53-1,(4S,5S,6S)-6-[(1R,2S,5R)-2-isopropyl-5-methylcyclohexyloxy]-4,5-isopropylidene-3-trifluoromethyl-5,6-dihydro-4H-1,2-oxazine

956350-53-1

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Basic information

Product Name: (4S,5S,6S)-6-[(1R,2S,5R)-2-isopropyl-5-methylcyclohexyloxy]-4,5-isopropylidene-3-trifluoromethyl-5,6-dihydro-4H-1,2-oxazine
Synonyms:
CAS NO:956350-53-1
Molecular Formula:
Molecular Weight: 379.42
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: (4S,5S,6S)-6-[(1R,2S,5R)-2-isopropyl-5-methylcyclohexyloxy]-4,5-isopropylidene-3-trifluoromethyl-5,6-dihydro-4H-1,2-oxazine(CAS DataBase Reference)
NIST Chemistry Reference: (4S,5S,6S)-6-[(1R,2S,5R)-2-isopropyl-5-methylcyclohexyloxy]-4,5-isopropylidene-3-trifluoromethyl-5,6-dihydro-4H-1,2-oxazine(956350-53-1)
EPA Substance Registry System: (4S,5S,6S)-6-[(1R,2S,5R)-2-isopropyl-5-methylcyclohexyloxy]-4,5-isopropylidene-3-trifluoromethyl-5,6-dihydro-4H-1,2-oxazine(956350-53-1)

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: 956350-53-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 956350-53-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,6,3,5 and 0 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 956350-53:
(8*9)+(7*5)+(6*6)+(5*3)+(4*5)+(3*0)+(2*5)+(1*3)=191
191 % 10 = 1
So 956350-53-1 is a valid CAS Registry Number.

956350-53-1Upstream product

77-76-9 2,2-dimethoxy-propane

956350-53-1Downstream Products

956350-53-1Relevant academic research and scientific papers

A stereoselective access to dihydroxylated pyrrolidines by reductive ring contraction of 1,2-oxazines

Reissig, Hans-Ulrich,Homann, Kai,Hiller, Florian,Zimmer, Reinhold

, p. 2681 - 2689 (2007)

Protected dihydroxylated 1,2-oxazine derivatives such as rac-4 were converted into tetrahydro-1,2-oxazines rac-7 by employing BH3· THF for the stereoselective reduction of the C=N bond. Compound 7a underwent a reductive ring contraction on hydr

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