Cas 238748-83-9,(9H-Fluoren-9-yl)methyl N-<(1S)-2-<<1,1-dimethyl-2-<methyl(phenyl)amino>-2-thioxoethyl>amino>-1-methyl-2-oxoethyl>carbamate

238748-83-9

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Basic information

Product Name: (9H-Fluoren-9-yl)methyl N-<(1S)-2-<<1,1-dimethyl-2--2-thioxoethyl>amino>-1-methyl-2-oxoethyl>carbamate
Synonyms:
CAS NO:238748-83-9
Molecular Formula:
Molecular Weight: 501.649
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: (9H-Fluoren-9-yl)methyl N-<(1S)-2-<<1,1-dimethyl-2--2-thioxoethyl>amino>-1-methyl-2-oxoethyl>carbamate(CAS DataBase Reference)
NIST Chemistry Reference: (9H-Fluoren-9-yl)methyl N-<(1S)-2-<<1,1-dimethyl-2--2-thioxoethyl>amino>-1-methyl-2-oxoethyl>carbamate(238748-83-9)
EPA Substance Registry System: (9H-Fluoren-9-yl)methyl N-<(1S)-2-<<1,1-dimethyl-2--2-thioxoethyl>amino>-1-methyl-2-oxoethyl>carbamate(238748-83-9)

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: 238748-83-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 238748-83-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,3,8,7,4 and 8 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 238748-83:
(8*2)+(7*3)+(6*8)+(5*7)+(4*4)+(3*8)+(2*8)+(1*3)=179
179 % 10 = 9
So 238748-83-9 is a valid CAS Registry Number.

238748-83-9Upstream product

238748-83-9Downstream Products

227612-08-0 (9H-Fluoren-9-yl)methyl N-<(1S)-2-<<1,1-dimethyl-2--2-oxoethyl>amino>-1-methyl-2-thioxoethyl>carbamate

238748-83-9Relevant academic research and scientific papers

A novel acid-catalyzed isomerization of Aib-containing thiodipeptides

Lehmann, Juerg,Linden, Anthony,Heimgartner, Heinz

, p. 888 - 908 (2007/10/03)

The use of amino thioacids in the 'azirine/oxazolone method' led to completely epimerized Aib-containing endothiodipeptides (Aib=2- aminoisobutyric acid). It could be established that the epimerization occurred during the acidic hydrolysis of the primaril

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