Cas 1907-80-8,2-(1-diethylcarbamoyl-ethyldisulfanyl)-N,N-diethyl-propionamide

1907-80-8

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Basic information

Product Name: 2-(1-diethylcarbamoyl-ethyldisulfanyl)-N,N-diethyl-propionamide
Synonyms: 2-(1-diethylcarbamoyl-ethyldisulfanyl)-N,N-diethyl-propionamide
CAS NO:1907-80-8
Molecular Formula:
Molecular Weight: 320.521
EINECS: N/A
Product Categories: N/A
Mol File: 1907-80-8.mol
Article Data: 1

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: 2-(1-diethylcarbamoyl-ethyldisulfanyl)-N,N-diethyl-propionamide(CAS DataBase Reference)
NIST Chemistry Reference: 2-(1-diethylcarbamoyl-ethyldisulfanyl)-N,N-diethyl-propionamide(1907-80-8)
EPA Substance Registry System: 2-(1-diethylcarbamoyl-ethyldisulfanyl)-N,N-diethyl-propionamide(1907-80-8)

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: 1907-80-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1907-80-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,0 and 7 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1907-80:
(6*1)+(5*9)+(4*0)+(3*7)+(2*8)+(1*0)=88
88 % 10 = 8
So 1907-80-8 is a valid CAS Registry Number.

1907-80-8Upstream product

4775-93-3 2,2'-dithiobispropanoic acid

1907-80-8Downstream Products

1907-80-8Relevant articles and documents

Dynamic kinetic resolution of amines involving biocatalysis and in situ free radical mediated racemization

Gastaldi, Stephane,Escoubet, Stephanie,Vanthuyne, Nicolas,Gil, Gerard,Bertrand, Michele P.

, p. 837 - 839 (2007)

(Chemical Equation Presented) The association of lipase-catalyzed enzymatic resolution with in situ racemization mediated with the thiyl radical enables the dynamic kinetic resolution of non-benzylic amines. It leads to (R)-amides with high enantioselectivities. It can be applied either to the conversion of racemic mixtures or to the inversion of (S)-enantiomers.

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