Cas 132532-95-7,4-phenyl-2-oxa-3-aza-r-1,c-5,c-6,c-7,t-8,t-11,c-12,c-13-pentacyclo<8.3.18,11.16,13.07,12>pentadeca-3,9-diene

132532-95-7

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Basic information

Product Name: 4-phenyl-2-oxa-3-aza-r-1,c-5,c-6,c-7,t-8,t-11,c-12,c-13-pentacyclo<8.3.1^8,11.1^6,13.0^7,12>pentadeca-3,9-diene
Synonyms:
CAS NO:132532-95-7
Molecular Formula:
Molecular Weight: 277.366
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: 4-phenyl-2-oxa-3-aza-r-1,c-5,c-6,c-7,t-8,t-11,c-12,c-13-pentacyclo<8.3.1^8,11.1^6,13.0^7,12>pentadeca-3,9-diene(CAS DataBase Reference)
NIST Chemistry Reference: 4-phenyl-2-oxa-3-aza-r-1,c-5,c-6,c-7,t-8,t-11,c-12,c-13-pentacyclo<8.3.1^8,11.1^6,13.0^7,12>pentadeca-3,9-diene(132532-95-7)
EPA Substance Registry System: 4-phenyl-2-oxa-3-aza-r-1,c-5,c-6,c-7,t-8,t-11,c-12,c-13-pentacyclo<8.3.1^8,11.1^6,13.0^7,12>pentadeca-3,9-diene(132532-95-7)

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: 132532-95-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 132532-95-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,5,3 and 2 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 132532-95:
(8*1)+(7*3)+(6*2)+(5*5)+(4*3)+(3*2)+(2*9)+(1*5)=107
107 % 10 = 7
So 132532-95-7 is a valid CAS Registry Number.

132532-95-7Upstream product

14783-85-8 3-phenyl-3a,4,7,7a-tetrahydro-4,7-methanobenzisoxazole

132532-95-7Downstream Products

132532-95-7Relevant academic research and scientific papers

Structure of a Norbornane-Fused Pentacyclic Isoxazoline

Sohar, Pal,Koevesdi, Istvan,Frimpong-Manso, Samuel,Stajer, Geza,Bernath, Gabor

, p. 1023 - 1026 (1990)

The steric structure of a pentacyclic adduct formed as a byproduct in a retro-Diels-Alder reaction was elucidated by 1H and 13C NMR spectroscopy, making use of double resonance and differential nuclear Overhauser effect measurements.

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