Cas 86087-20-9,(1R,2S)-1-Benzyloxycarbonylamino-2-phenyl-cyclopropanecarboxylic acid

86087-20-9

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Basic information

Product Name: (1R,2S)-1-Benzyloxycarbonylamino-2-phenyl-cyclopropanecarboxylic acid
Synonyms: (1R,2S)-1-Benzyloxycarbonylamino-2-phenyl-cyclopropanecarboxylic acid
CAS NO:86087-20-9
Molecular Formula:
Molecular Weight: 311.337
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: (1R,2S)-1-Benzyloxycarbonylamino-2-phenyl-cyclopropanecarboxylic acid(CAS DataBase Reference)
NIST Chemistry Reference: (1R,2S)-1-Benzyloxycarbonylamino-2-phenyl-cyclopropanecarboxylic acid(86087-20-9)
EPA Substance Registry System: (1R,2S)-1-Benzyloxycarbonylamino-2-phenyl-cyclopropanecarboxylic acid(86087-20-9)

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: 86087-20-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 86087-20-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,0,8 and 7 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 86087-20:
(7*8)+(6*6)+(5*0)+(4*8)+(3*7)+(2*2)+(1*0)=149
149 % 10 = 9
So 86087-20-9 is a valid CAS Registry Number.

86087-20-9Upstream product

86087-20-9Downstream Products

86087-20-9Relevant academic research and scientific papers

A formyl peptide substituted with a conformationally constrained phenylalanine residue evokes a selective immune response in human neutrophils

Hayashi, Ryo,Miyazaki, Masaya,Osada, Satoshi,Kawasaki, Hiroshi,Fujita, Ichiro,Hamasaki, Yuhei,Kodama, Hiroaki

supporting information, p. 668 - 675 (2013/02/25)

Formyl-Met-Leu-Phe-OH (fMLP) binds to formyl peptide receptors, FPR1 and FPR2, and evokes migration and superoxide anion production in human neutrophils. To obtain a more effective and selective ligand, fMLP analogs in which the Phe residue was substitute

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