Cas 8545-55-9,2-phenylcyclopropanone 1,3-(2,2-dimethyl)propanediyl acetal

8545-55-9

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Basic information

Product Name: 2-phenylcyclopropanone 1,3-(2,2-dimethyl)propanediyl acetal
Synonyms: 2-phenylcyclopropanone 1,3-(2,2-dimethyl)propanediyl acetal
CAS NO:8545-55-9
Molecular Formula:
Molecular Weight: 218.296
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-phenylcyclopropanone 1,3-(2,2-dimethyl)propanediyl acetal(CAS DataBase Reference)
NIST Chemistry Reference: 2-phenylcyclopropanone 1,3-(2,2-dimethyl)propanediyl acetal(8545-55-9)
EPA Substance Registry System: 2-phenylcyclopropanone 1,3-(2,2-dimethyl)propanediyl acetal(8545-55-9)

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: 8545-55-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 8545-55-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 8,5,4 and 5 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 8545-55:
(6*8)+(5*5)+(4*4)+(3*5)+(2*5)+(1*5)=119
119 % 10 = 9
So 8545-55-9 is a valid CAS Registry Number.

8545-55-9Upstream product

60935-22-0 6,6-dimethyl-4,8-dioxaspiro[2,5]oct-1-ene

8545-55-9Downstream Products

8545-55-9Relevant academic research and scientific papers

Synthesis of substituted cyclopropanone acetals by carbometallation and its oxidative cleavage with manganese(IV) oxide and lead(IV) oxide

Nakamura, Masaharu,Inoue, Toshihiro,Nakamura, Eiichi

, p. 300 - 306 (2001)

A variety of substituted cyclopropanone acetals were prepared by the addition of an organozinc reagent or a Grignard reagent to a substituted cyclopropenone acetal. MnO2- or PbO2-mediated oxidative ring opening reaction of the substituted cyclopropanone acetals affords β-alkoxyesters and protected β-aminoesters with high efficiency.

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