Cas 155501-30-7,2-[3-((1S,6R)-6-p-Tolylsulfanyl-bicyclo[4.1.0]hept-1-yl)-propylidene]-malonic acid diethyl ester

155501-30-7

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Basic information

Product Name: 2-[3-((1S,6R)-6-p-Tolylsulfanyl-bicyclo[4.1.0]hept-1-yl)-propylidene]-malonic acid diethyl ester
Synonyms: 2-[3-((1S,6R)-6-p-Tolylsulfanyl-bicyclo[4.1.0]hept-1-yl)-propylidene]-malonic acid diethyl ester
CAS NO:155501-30-7
Molecular Formula:
Molecular Weight: 416.582
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-((1S,6R)-6-p-Tolylsulfanyl-bicyclo[4.1.0]hept-1-yl)-propylidene]-malonic acid diethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 2-[3-((1S,6R)-6-p-Tolylsulfanyl-bicyclo[4.1.0]hept-1-yl)-propylidene]-malonic acid diethyl ester(155501-30-7)
EPA Substance Registry System: 2-[3-((1S,6R)-6-p-Tolylsulfanyl-bicyclo[4.1.0]hept-1-yl)-propylidene]-malonic acid diethyl ester(155501-30-7)

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: 155501-30-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 155501-30-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,5,5,0 and 1 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 155501-30:
(8*1)+(7*5)+(6*5)+(5*5)+(4*0)+(3*1)+(2*3)+(1*0)=107
107 % 10 = 7
So 155501-30-7 is a valid CAS Registry Number.

155501-30-7Upstream product

155501-30-7Downstream Products

155501-30-7Relevant academic research and scientific papers

Novel Intramolecular Michael Addition of Organomercury Halides Mediated by a Lewis Acid and Halide Anion

Takemoto, Yoshiji,Ohra, Taiichi,Yonetoku, Yasuhiro,Nishimine, Kazumi,Iwata, Chuzo

, p. 81 - 82 (1994)

Alkylmercury chloride bearing electron-deficient olefin 3 undergoes a Michael reaction intramolecularly via hypervalent intermediates 10 by the double activation method mediated by a Lewis acid and iodide anion to provide spirocyclic compounds 4 and 5.

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