Cas 3454-82-8,1-Phenethyl-cyclopropanecarbonyl chloride

3454-82-8

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Basic information

Product Name: 1-Phenethyl-cyclopropanecarbonyl chloride
Synonyms:
CAS NO:3454-82-8
Molecular Formula:
Molecular Weight: 208.688
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: 1-Phenethyl-cyclopropanecarbonyl chloride(CAS DataBase Reference)
NIST Chemistry Reference: 1-Phenethyl-cyclopropanecarbonyl chloride(3454-82-8)
EPA Substance Registry System: 1-Phenethyl-cyclopropanecarbonyl chloride(3454-82-8)

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: 3454-82-8(Hazardous Substances Data)

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3454-82-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3454-82-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,5 and 4 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3454-82:
(6*3)+(5*4)+(4*5)+(3*4)+(2*8)+(1*2)=88
88 % 10 = 8
So 3454-82-8 is a valid CAS Registry Number.

3454-82-8Upstream product

3454-82-8Downstream Products

1346641-01-7 N-(4-cyano-2,3,5,6-tetrafluorophenyl)-1-phenethylcyclopropanecarboxamide

3454-82-8Relevant academic research and scientific papers

Pd(II)-catalyzed enantioselective C-H activation of cyclopropanes

Wasa, Masayuki,Engle, Keary M.,Lin, David W.,Yoo, Eun Jeong,Yu, Jin-Quan

, p. 19598 - 19601 (2012/01/17)

Systematic ligand development has led to the identification of novel mono-N-protected amino acid ligands for Pd(II)-catalyzed enantioselective C-H activation of cyclopropanes. A diverse range of organoboron reagents can be used as coupling partners, and the reaction proceeds under mild conditions. These results provide a new retrosynthetic disconnection for the construction of enantioenriched cis-substituted cyclopropanecarboxylic acids.

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