Cas 172992-11-9,(S)-2-{1-[(S)-1-(1-Methoxycarbonyl-1-methyl-ethylcarbamoyl)-ethylcarbamoyl]-1-methyl-ethylcarbamoyl}-pyrrolidine-1-carboxylic acid benzyl ester

172992-11-9

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Basic information

Product Name: (S)-2-{1-[(S)-1-(1-Methoxycarbonyl-1-methyl-ethylcarbamoyl)-ethylcarbamoyl]-1-methyl-ethylcarbamoyl}-pyrrolidine-1-carboxylic acid benzyl ester
Synonyms:
CAS NO:172992-11-9
Molecular Formula:
Molecular Weight: 504.583
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-{1-[(S)-1-(1-Methoxycarbonyl-1-methyl-ethylcarbamoyl)-ethylcarbamoyl]-1-methyl-ethylcarbamoyl}-pyrrolidine-1-carboxylic acid benzyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (S)-2-{1-[(S)-1-(1-Methoxycarbonyl-1-methyl-ethylcarbamoyl)-ethylcarbamoyl]-1-methyl-ethylcarbamoyl}-pyrrolidine-1-carboxylic acid benzyl ester(172992-11-9)
EPA Substance Registry System: (S)-2-{1-[(S)-1-(1-Methoxycarbonyl-1-methyl-ethylcarbamoyl)-ethylcarbamoyl]-1-methyl-ethylcarbamoyl}-pyrrolidine-1-carboxylic acid benzyl ester(172992-11-9)

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: 172992-11-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 172992-11-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,2,9,9 and 2 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 172992-11:
(8*1)+(7*7)+(6*2)+(5*9)+(4*9)+(3*2)+(2*1)+(1*1)=159
159 % 10 = 9
So 172992-11-9 is a valid CAS Registry Number.

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172992-11-9Relevant academic research and scientific papers

Efficient synthesis of alamethicin F-30 using a chloro imidazolidium coupling reagent, CIP

Akaji, Kenichi,Tamai, Yasunori,Kiso, Yoshiaki

, p. 9341 - 9344 (2007/10/02)

Alamethicin F-30 has been synthesized in solution using a CIP-additive as a coupling agent and TFA as a final deprotecting reagent. All couplings including those between sterically hindered α,α-dimethyl amino acid were successfully achieved by a 60 min re

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