Cas 861632-17-9,N-[[[(2-propenyloxy)carbonyl]-N'-(benzyl)amino]sulfonyl]-N-(2-propenyl)-(S)-leucine methyl ester

861632-17-9

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Basic information

Product Name: N-[[[(2-propenyloxy)carbonyl]-N'-(benzyl)amino]sulfonyl]-N-(2-propenyl)-(S)-leucine methyl ester
Synonyms: N-[[[(2-propenyloxy)carbonyl]-N'-(benzyl)amino]sulfonyl]-N-(2-propenyl)-(S)-leucine methyl ester
CAS NO:861632-17-9
Molecular Formula:
Molecular Weight: 438.545
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: N-[[[(2-propenyloxy)carbonyl]-N'-(benzyl)amino]sulfonyl]-N-(2-propenyl)-(S)-leucine methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: N-[[[(2-propenyloxy)carbonyl]-N'-(benzyl)amino]sulfonyl]-N-(2-propenyl)-(S)-leucine methyl ester(861632-17-9)
EPA Substance Registry System: N-[[[(2-propenyloxy)carbonyl]-N'-(benzyl)amino]sulfonyl]-N-(2-propenyl)-(S)-leucine methyl ester(861632-17-9)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 861632-17-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 861632-17-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,1,6,3 and 2 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 861632-17:
(8*8)+(7*6)+(6*1)+(5*6)+(4*3)+(3*2)+(2*1)+(1*7)=169
169 % 10 = 9
So 861632-17-9 is a valid CAS Registry Number.

861632-17-9Upstream product

861632-17-9Downstream Products

861632-17-9Relevant academic research and scientific papers

Synthesis of cyclic sulfamoyl carbamates and ureas via ring-closing metathesis

Dougherty, Joseph M.,Jiménez, María,Hanson, Paul R.

, p. 6218 - 6230 (2007/10/03)

Synthetic routes to a diverse set of cyclic sulfamoyl carbamates and ureas are reported. These routes utilize 3-component coupling, Mitsunobu alkylation, and ring-closing metathesis using the second-generation Grubbs catalyst to achieve the synthesis of t

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