Cas 139715-24-5,(4aR,5R,11bR)-5,7-Diphenyl-3,4,5,11b-tetrahydro-1H-2-oxa-4a-aza-dibenzo[a,c]cycloheptene

139715-24-5

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Basic information

Product Name: (4aR,5R,11bR)-5,7-Diphenyl-3,4,5,11b-tetrahydro-1H-2-oxa-4a-aza-dibenzo[a,c]cycloheptene
Synonyms:
CAS NO:139715-24-5
Molecular Formula:
Molecular Weight: 353.464
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: (4aR,5R,11bR)-5,7-Diphenyl-3,4,5,11b-tetrahydro-1H-2-oxa-4a-aza-dibenzo[a,c]cycloheptene(CAS DataBase Reference)
NIST Chemistry Reference: (4aR,5R,11bR)-5,7-Diphenyl-3,4,5,11b-tetrahydro-1H-2-oxa-4a-aza-dibenzo[a,c]cycloheptene(139715-24-5)
EPA Substance Registry System: (4aR,5R,11bR)-5,7-Diphenyl-3,4,5,11b-tetrahydro-1H-2-oxa-4a-aza-dibenzo[a,c]cycloheptene(139715-24-5)

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: 139715-24-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 139715-24-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,9,7,1 and 5 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 139715-24:
(8*1)+(7*3)+(6*9)+(5*7)+(4*1)+(3*5)+(2*2)+(1*4)=145
145 % 10 = 5
So 139715-24-5 is a valid CAS Registry Number.

139715-24-5Upstream product

131319-47-6 4-Triphenylpropa-1,2-dienyl-morpholine

139715-24-5Downstream Products

139715-24-5Relevant academic research and scientific papers

THERMAL ISOMERIZATION OF 1-MORPHOLINO-3-PHEHYL (OR VINYL)-ALLENES: SYNTHESIS OF THE OXAZINOAZEPINE FRAMEWORK

Mayer, Theo,Maas, Gerhard

, p. 205 - 208 (1992)

1-Morpholino-3-phenylallenes isomerize to 3,4,6,12b-tetrahydro-1H-oxazinobenzazepines at >/= 105 deg C.Similarly, 1-morpholino-3-vinylallenes are transformed into 3,4,10,10a-tetrahydro-1H-oxazinoazepines.Formation of these novel heterocycles is rationalized by a 1,3-proton shift in the morpholinoallenes, followed by 1,7-electrocylization of the α,β,γ,δ-unsaturated azomethine ylide thus formed.

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