Cas 936444-99-4,(3R,6R,7R,9aS)-3-(azidomethyl)-6-(4-bromophenyl)-7-methyl-hexahydropyrido[2,1-c][1,4]oxazin-1(6H)-one

936444-99-4

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Basic information

Product Name: (3R,6R,7R,9aS)-3-(azidomethyl)-6-(4-bromophenyl)-7-methyl-hexahydropyrido[2,1-c][1,4]oxazin-1(6H)-one
Synonyms: (3R,6R,7R,9aS)-3-(azidomethyl)-6-(4-bromophenyl)-7-methyl-hexahydropyrido[2,1-c][1,4]oxazin-1(6H)-one
CAS NO:936444-99-4
Molecular Formula:
Molecular Weight: 379.256
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,6R,7R,9aS)-3-(azidomethyl)-6-(4-bromophenyl)-7-methyl-hexahydropyrido[2,1-c][1,4]oxazin-1(6H)-one(CAS DataBase Reference)
NIST Chemistry Reference: (3R,6R,7R,9aS)-3-(azidomethyl)-6-(4-bromophenyl)-7-methyl-hexahydropyrido[2,1-c][1,4]oxazin-1(6H)-one(936444-99-4)
EPA Substance Registry System: (3R,6R,7R,9aS)-3-(azidomethyl)-6-(4-bromophenyl)-7-methyl-hexahydropyrido[2,1-c][1,4]oxazin-1(6H)-one(936444-99-4)

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: 936444-99-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 936444-99-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,3,6,4,4 and 4 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 936444-99:
(8*9)+(7*3)+(6*6)+(5*4)+(4*4)+(3*4)+(2*9)+(1*9)=204
204 % 10 = 4
So 936444-99-4 is a valid CAS Registry Number.

936444-99-4Upstream product

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936444-99-4Relevant academic research and scientific papers

Stereochemical and skeletal diversity employing pipecolate ester scaffolds

Yu, Chen,Porco Jr., John A.,Panek, James S.

, p. 1529 - 1532 (2008/02/02)

Equation presented The stereocontrolled synthesis of pyridooxazinones by Mg(OTf)2-promoted epoxide ring-opening with use of chiral pipecolates as nucleophiles is described. Pyridooxazinone products derived from azido-epoxides can be further rea

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