Cas 1394239-84-9,(S)-2-((S)-2-((tert-butoxycarbonyl)amino)-3-phenylpropanamido)-3-phenylpropyl pyrrolidine-1-carbodithioate

1394239-84-9

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Basic information

Product Name: (S)-2-((S)-2-((tert-butoxycarbonyl)amino)-3-phenylpropanamido)-3-phenylpropyl pyrrolidine-1-carbodithioate
Synonyms:
CAS NO:1394239-84-9
Molecular Formula:
Molecular Weight: 527.752
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-((S)-2-((tert-butoxycarbonyl)amino)-3-phenylpropanamido)-3-phenylpropyl pyrrolidine-1-carbodithioate(CAS DataBase Reference)
NIST Chemistry Reference: (S)-2-((S)-2-((tert-butoxycarbonyl)amino)-3-phenylpropanamido)-3-phenylpropyl pyrrolidine-1-carbodithioate(1394239-84-9)
EPA Substance Registry System: (S)-2-((S)-2-((tert-butoxycarbonyl)amino)-3-phenylpropanamido)-3-phenylpropyl pyrrolidine-1-carbodithioate(1394239-84-9)

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: 1394239-84-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1394239-84-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,9,4,2,3 and 9 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1394239-84:
(9*1)+(8*3)+(7*9)+(6*4)+(5*2)+(4*3)+(3*9)+(2*8)+(1*4)=189
189 % 10 = 9
So 1394239-84-9 is a valid CAS Registry Number.

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1394239-84-9Relevant academic research and scientific papers

A modular synthesis of dithiocarbamate pendant unnatural α-amino acids

Saha, Amit,Baig, R. B. Nasir,Leazer, John,Varma, Rajender S.

, p. 8889 - 8891 (2012/11/07)

Unnatural α-amino acids containing dithiocarbamate side chains were synthesized by a one-pot reaction of in situ generated dithiocarbamate anions with sulfamidates. A wide range of these anions participated in the highly regio- and stereo-selective ring opening of sulfamidates to produce the corresponding dithiocarbamate pendant α-amino acids in high yields.

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