Cas 1357309-68-2,(1R,2S,3R)-3-(formyloxy)-1-[(R)-2-methyl-6,6-diphenyl-5,6-dihydro-4H-1,3-oxazin-4-yl]butane-1,2,4-triyl triacetate

1357309-68-2

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Basic information

Product Name: (1R,2S,3R)-3-(formyloxy)-1-[(R)-2-methyl-6,6-diphenyl-5,6-dihydro-4H-1,3-oxazin-4-yl]butane-1,2,4-triyl triacetate
Synonyms:
CAS NO:1357309-68-2
Molecular Formula:
Molecular Weight: 525.555
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: (1R,2S,3R)-3-(formyloxy)-1-[(R)-2-methyl-6,6-diphenyl-5,6-dihydro-4H-1,3-oxazin-4-yl]butane-1,2,4-triyl triacetate(CAS DataBase Reference)
NIST Chemistry Reference: (1R,2S,3R)-3-(formyloxy)-1-[(R)-2-methyl-6,6-diphenyl-5,6-dihydro-4H-1,3-oxazin-4-yl]butane-1,2,4-triyl triacetate(1357309-68-2)
EPA Substance Registry System: (1R,2S,3R)-3-(formyloxy)-1-[(R)-2-methyl-6,6-diphenyl-5,6-dihydro-4H-1,3-oxazin-4-yl]butane-1,2,4-triyl triacetate(1357309-68-2)

Safety Data

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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1357309-68-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1357309-68-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,7,3,0 and 9 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1357309-68:
(9*1)+(8*3)+(7*5)+(6*7)+(5*3)+(4*0)+(3*9)+(2*6)+(1*8)=172
172 % 10 = 2
So 1357309-68-2 is a valid CAS Registry Number.

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1357309-68-2Relevant academic research and scientific papers

One-pot conversion of serine derivatives and amino sugars into oxazine derivatives of γ-aryl-γ-(hydroxy)amines

Boto, Alicia,Gallardo, Juan A.,Alvarez, Eleuterio

experimental part, p. 391 - 397 (2012/03/09)

A one-pot process for the transformation of relatively inexpensive serine derivatives into oxazine derivatives of γ-aryl-γ-hydroxy-α- amino acids is described. The reaction preferentially afforded 4,6-cis oxazines. The method can also be applied to the tr

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