Cas 13522-99-1,2',3,10'-trimethoxy-5-phenyl-4',8'-diphenylspiro[cyclohexane-1,6'-dibenzo[d,f][1,3]dioxepine]-2,4-dien-6-one

13522-99-1

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Basic information

Product Name: 2',3,10'-trimethoxy-5-phenyl-4',8'-diphenylspiro[cyclohexane-1,6'-dibenzo[d,f][1,3]dioxepine]-2,4-dien-6-one
Synonyms: 2',3,10'-trimethoxy-5-phenyl-4',8'-diphenylspiro[cyclohexane-1,6'-dibenzo[d,f][1,3]dioxepine]-2,4-dien-6-one
CAS NO:13522-99-1
Molecular Formula:
Molecular Weight: 594.664
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: 2',3,10'-trimethoxy-5-phenyl-4',8'-diphenylspiro[cyclohexane-1,6'-dibenzo[d,f][1,3]dioxepine]-2,4-dien-6-one(CAS DataBase Reference)
NIST Chemistry Reference: 2',3,10'-trimethoxy-5-phenyl-4',8'-diphenylspiro[cyclohexane-1,6'-dibenzo[d,f][1,3]dioxepine]-2,4-dien-6-one(13522-99-1)
EPA Substance Registry System: 2',3,10'-trimethoxy-5-phenyl-4',8'-diphenylspiro[cyclohexane-1,6'-dibenzo[d,f][1,3]dioxepine]-2,4-dien-6-one(13522-99-1)

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: 13522-99-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 13522-99-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,5,2 and 2 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 13522-99:
(7*1)+(6*3)+(5*5)+(4*2)+(3*2)+(2*9)+(1*9)=91
91 % 10 = 1
So 13522-99-1 is a valid CAS Registry Number.

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13522-99-1Relevant academic research and scientific papers

Total Synthesis of Pyrolaside B: Phenol Trimerization through Sequenced Oxidative C?C and C?O Coupling

Kozlowski, Marisa C.,Neuhaus, William C.

, p. 7842 - 7847 (2020/04/03)

A facile method to oxidatively trimerize phenols using a catalytic aerobic copper system is described. The mechanism of this transformation was probed, yielding insight that enabled cross-coupling trimerizations. With this method, the natural product pyro

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