Cas 226923-12-2,8-bromo-3-phenyl-2,3,6,8a-tetrahydro-5<i>H</i>-oxazolo[3,2-<i>a</i>]pyridine-5-carbonitrile

226923-12-2

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Basic information

Product Name: 8-bromo-3-phenyl-2,3,6,8a-tetrahydro-5H-oxazolo[3,2-a]pyridine-5-carbonitrile
Synonyms: 8-bromo-3-phenyl-2,3,6,8a-tetrahydro-5H-oxazolo[3,2-a]pyridine-5-carbonitrile
CAS NO:226923-12-2
Molecular Formula:
Molecular Weight: 305.174
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: 8-bromo-3-phenyl-2,3,6,8a-tetrahydro-5H-oxazolo[3,2-a]pyridine-5-carbonitrile(CAS DataBase Reference)
NIST Chemistry Reference: 8-bromo-3-phenyl-2,3,6,8a-tetrahydro-5H-oxazolo[3,2-a]pyridine-5-carbonitrile(226923-12-2)
EPA Substance Registry System: 8-bromo-3-phenyl-2,3,6,8a-tetrahydro-5H-oxazolo[3,2-a]pyridine-5-carbonitrile(226923-12-2)

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: 226923-12-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 226923-12-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,6,9,2 and 3 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 226923-12:
(8*2)+(7*2)+(6*6)+(5*9)+(4*2)+(3*3)+(2*1)+(1*2)=132
132 % 10 = 2
So 226923-12-2 is a valid CAS Registry Number.

226923-12-2Upstream product

226923-12-2Downstream Products

226923-14-4 (3R,5S,7S,8S,8aR)-8-Bromo-7-methoxy-3-phenyl-hexahydro-oxazolo[3,2-a]pyridine-5-carbonitrile

226923-12-2Relevant academic research and scientific papers

Asymmetric synthesis of polyfunctionalized piperidines: Substitution at the C-4 position

Billon-Souquet, Florence,Martens, Thierry,Royer, Jacques

, p. 3731 - 3734 (1999)

The electrochemical bis-bromination of the chiral building block I followed by a dehydrobromination step allowed the preparation of a bromopiperideine 3. The stereoselective addition of nucleophiles onto this key intermediate permitted the synthesis of va

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