Cas 364802-19-7,(S)-2-{(2-Azido-benzyl)-[(E)-(3-phenyl-acryloyl)]-amino}-propionic acid benzyl ester

364802-19-7

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Basic information

Product Name: (S)-2-{(2-Azido-benzyl)-[(E)-(3-phenyl-acryloyl)]-amino}-propionic acid benzyl ester
Synonyms: (S)-2-{(2-Azido-benzyl)-[(E)-(3-phenyl-acryloyl)]-amino}-propionic acid benzyl ester
CAS NO:364802-19-7
Molecular Formula:
Molecular Weight: 440.502
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: (S)-2-{(2-Azido-benzyl)-[(E)-(3-phenyl-acryloyl)]-amino}-propionic acid benzyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (S)-2-{(2-Azido-benzyl)-[(E)-(3-phenyl-acryloyl)]-amino}-propionic acid benzyl ester(364802-19-7)
EPA Substance Registry System: (S)-2-{(2-Azido-benzyl)-[(E)-(3-phenyl-acryloyl)]-amino}-propionic acid benzyl ester(364802-19-7)

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: 364802-19-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 364802-19-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,6,4,8,0 and 2 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 364802-19:
(8*3)+(7*6)+(6*4)+(5*8)+(4*0)+(3*2)+(2*1)+(1*9)=147
147 % 10 = 7
So 364802-19-7 is a valid CAS Registry Number.

364802-19-7Upstream product

364802-19-7Downstream Products

946533-92-2 2-benzyl-4-[1-(S)-(benzyloxycarbonyl)ethyl]-4,5-dihydro-1,4-benzodiazepin-3-one

364802-19-7Relevant academic research and scientific papers

Stereoselective intramolecular cycloadditions of homochiral N-alkenoyl aryl azides

Broggini, Gianluigi,Garanti, Luisa,Molteni, Giorgio,Pilati, Tullio

, p. 1201 - 1206 (2007/10/03)

Starting from the commercially available (S)-1-phenylethylamine and L-alanine benzylester, we synthesised the homochiral N-alkenoyl aryl azides 2a-2d. The intramolecular cycloaddition of unsubstituted 2a and 2b gave enantiopure 3,3a-dihydro-1,2,3-triazolo

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