Cas 1101-55-9,7,7-Diphenyl-p-mentha-1<sup>(7)</sup>,2,5-trien-8-carbonsaere-methylester

1101-55-9

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Basic information

Product Name: 7,7-Diphenyl-p-mentha-1⁽⁷⁾,2,5-trien-8-carbonsaere-methylester
Synonyms: 7,7-Diphenyl-p-mentha-1⁽⁷⁾,2,5-trien-8-carbonsaere-methylester
CAS NO:1101-55-9
Molecular Formula:
Molecular Weight: 344.453
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: 7,7-Diphenyl-p-mentha-1⁽⁷⁾,2,5-trien-8-carbonsaere-methylester(CAS DataBase Reference)
NIST Chemistry Reference: 7,7-Diphenyl-p-mentha-1⁽⁷⁾,2,5-trien-8-carbonsaere-methylester(1101-55-9)
EPA Substance Registry System: 7,7-Diphenyl-p-mentha-1⁽⁷⁾,2,5-trien-8-carbonsaere-methylester(1101-55-9)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1101-55-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1101-55-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,0 and 1 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1101-55:
(6*1)+(5*1)+(4*0)+(3*1)+(2*5)+(1*5)=29
29 % 10 = 9
So 1101-55-9 is a valid CAS Registry Number.

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1101-55-9Downstream Products

1101-55-9Relevant academic research and scientific papers

Hydride Eliminations, IX. - Aromatization of Arenocyclohexanones

Reetz, Manfred T.,Stephan, Wilfried

, p. 533 - 541 (2007/10/02)

Arenocyclohexanones 1 can be aromatized via their silyl enol ethers 2 to phenol derivates 5 with the aid of trityl salts 7, or 2,6-dichloro-3,5-dicyano-p-benzoquinone (6a) or tetrachloro-p-benzoquinone (6b).The method is distinctly milder than classical aromatizations utilizing sulfur, selenium or metal catalysts.The method cannot be applied to aliphatic silyl enol ethers for obtaining α,β-unsaturated carbonyl compounds.Rather, one observes in certain cases α-tritylations.

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