Cas 124462-31-3,4,4a,5,6,7,8,9,9a-octahydro-3-phenyl-9a-(trimethylsiloxy)cyclohept<e>-1,2-oxazine

124462-31-3

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Basic information

Product Name: 4,4a,5,6,7,8,9,9a-octahydro-3-phenyl-9a-(trimethylsiloxy)cyclohept-1,2-oxazine
Synonyms: 4,4a,5,6,7,8,9,9a-octahydro-3-phenyl-9a-(trimethylsiloxy)cyclohept-1,2-oxazine
CAS NO:124462-31-3
Molecular Formula:
Molecular Weight: 317.503
EINECS: N/A
Product Categories: N/A
Mol File: 124462-31-3.mol
Article Data: 1

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: 4,4a,5,6,7,8,9,9a-octahydro-3-phenyl-9a-(trimethylsiloxy)cyclohept-1,2-oxazine(CAS DataBase Reference)
NIST Chemistry Reference: 4,4a,5,6,7,8,9,9a-octahydro-3-phenyl-9a-(trimethylsiloxy)cyclohept-1,2-oxazine(124462-31-3)
EPA Substance Registry System: 4,4a,5,6,7,8,9,9a-octahydro-3-phenyl-9a-(trimethylsiloxy)cyclohept-1,2-oxazine(124462-31-3)

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: 124462-31-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 124462-31-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,4,6 and 2 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 124462-31:
(8*1)+(7*2)+(6*4)+(5*4)+(4*6)+(3*2)+(2*3)+(1*1)=103
103 % 10 = 3
So 124462-31-3 is a valid CAS Registry Number.

124462-31-3Upstream product

124462-31-3Downstream Products

124462-31-3Relevant articles and documents

Synthesis of Trialkylsiloxy-Substituted and other 5,6-Dihydro-4H-1,2-oxazines by Hetero Diels-Alder Reactions of Nitroso Alkenes - Preparative Scope and Diastereoselectivity

Hippeli, Claudia,Reissig, Hans-Ulrich

, p. 217 - 226 (2007/10/02)

A variety of 5,6-dihydro-4H-1,2-oxazines 3 and 4 is prepared in good yields from silyl enol ethers 1 and nitroso alkenes 2a or 2b, respectively.A systematic variation of substitutens reveals preparative scope and limitations of this hetero Diels-Alder rea

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