Cas 6366-28-5,2-Benzoyl-1,1-bis-ethoxycarbonyl-cyclopropan

6366-28-5

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Basic information

Product Name: 2-Benzoyl-1,1-bis-ethoxycarbonyl-cyclopropan
Synonyms: 2-Benzoyl-1,1-bis-ethoxycarbonyl-cyclopropan
CAS NO:6366-28-5
Molecular Formula:
Molecular Weight: 290.316
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-Benzoyl-1,1-bis-ethoxycarbonyl-cyclopropan(CAS DataBase Reference)
NIST Chemistry Reference: 2-Benzoyl-1,1-bis-ethoxycarbonyl-cyclopropan(6366-28-5)
EPA Substance Registry System: 2-Benzoyl-1,1-bis-ethoxycarbonyl-cyclopropan(6366-28-5)

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: 6366-28-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 6366-28-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,6 and 6 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6366-28:
(6*6)+(5*3)+(4*6)+(3*6)+(2*2)+(1*8)=105
105 % 10 = 5
So 6366-28-5 is a valid CAS Registry Number.

6366-28-5Upstream product

3709-23-7 <3-Phenyl-3-oxo-propyl>-malonsaeure-diethylester

6366-28-5Downstream Products

6366-28-5Relevant academic research and scientific papers

Base-controlled selective conversion of Michael adducts of malonates with enones in the presence of iodine

Miao, Chun-Bao,Zhang, Min,Tian, Zong-Yong,Xi, Hai-Tao,Sun, Xiao-Qiang,Yang, Hai-Tao

experimental part, p. 9809 - 9816 (2012/01/06)

An efficient base-controlled selective conversion of the Michael adducts of malonates with enones in the presence of iodine is reported. Highly functionalized cyclopropane, oxetane, and α-hydroxylmalonate derivatives are obtained selectively using DBU, Na2CO3, and NaOAc as the base, respectively. O2 was identified to be crucial to the formation of oxetane and α-hydroxylmalonate derivatives.

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