Cas 918307-19-4,tert-butyl (1S)-1-((benzyl((1S)-1-benzylprop-2-en-1-yl)amino)carbonyl)but-3-en-1-yl)carbamate

918307-19-4

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Basic information

Product Name: tert-butyl (1S)-1-((benzyl((1S)-1-benzylprop-2-en-1-yl)amino)carbonyl)but-3-en-1-yl)carbamate
Synonyms: tert-butyl (1S)-1-((benzyl((1S)-1-benzylprop-2-en-1-yl)amino)carbonyl)but-3-en-1-yl)carbamate
CAS NO:918307-19-4
Molecular Formula:
Molecular Weight: 434.579
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: tert-butyl (1S)-1-((benzyl((1S)-1-benzylprop-2-en-1-yl)amino)carbonyl)but-3-en-1-yl)carbamate(CAS DataBase Reference)
NIST Chemistry Reference: tert-butyl (1S)-1-((benzyl((1S)-1-benzylprop-2-en-1-yl)amino)carbonyl)but-3-en-1-yl)carbamate(918307-19-4)
EPA Substance Registry System: tert-butyl (1S)-1-((benzyl((1S)-1-benzylprop-2-en-1-yl)amino)carbonyl)but-3-en-1-yl)carbamate(918307-19-4)

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: 918307-19-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 918307-19-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,8,3,0 and 7 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 918307-19:
(8*9)+(7*1)+(6*8)+(5*3)+(4*0)+(3*7)+(2*1)+(1*9)=174
174 % 10 = 4
So 918307-19-4 is a valid CAS Registry Number.

918307-19-4Upstream product

918307-19-4Downstream Products

918307-20-7 tert-butyl ((3S,7S)-1,7-dibenzyl-2-oxo-2,3,4,7-tetrahydro-1H-azepin-3-yl)carbamate

918307-19-4Relevant academic research and scientific papers

Synthesis of amino acid derived seven-membered lactams by RCM and their evaluation against HIV protease

Zaman, Shazia,Campaner, Pietro,Abell, Andrew D.

, p. 8323 - 8331 (2006)

A versatile synthesis of hydroxylated and epoxy 1-azepin 2-ones substituted at N1, C-3 and C-4 or C-7 has been developed. The sequence involves ring-closing metathesis of an amino acid derived diene amide, followed by either epoxidation or dihydroxylation

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