Cas 177659-56-2,(S)-1-[(S)-2-(tert-Butoxycarbonyl-methyl-amino)-pentanoyl]-pyrrolidine-2-carboxylic acid benzyl ester

177659-56-2

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Basic information

Product Name: (S)-1-[(S)-2-(tert-Butoxycarbonyl-methyl-amino)-pentanoyl]-pyrrolidine-2-carboxylic acid benzyl ester
Synonyms: (S)-1-[(S)-2-(tert-Butoxycarbonyl-methyl-amino)-pentanoyl]-pyrrolidine-2-carboxylic acid benzyl ester
CAS NO:177659-56-2
Molecular Formula:
Molecular Weight: 418.533
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)-1-[(S)-2-(tert-Butoxycarbonyl-methyl-amino)-pentanoyl]-pyrrolidine-2-carboxylic acid benzyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (S)-1-[(S)-2-(tert-Butoxycarbonyl-methyl-amino)-pentanoyl]-pyrrolidine-2-carboxylic acid benzyl ester(177659-56-2)
EPA Substance Registry System: (S)-1-[(S)-2-(tert-Butoxycarbonyl-methyl-amino)-pentanoyl]-pyrrolidine-2-carboxylic acid benzyl ester(177659-56-2)

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: 177659-56-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 177659-56-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,7,6,5 and 9 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 177659-56:
(8*1)+(7*7)+(6*7)+(5*6)+(4*5)+(3*9)+(2*5)+(1*6)=192
192 % 10 = 2
So 177659-56-2 is a valid CAS Registry Number.

177659-56-2Upstream product

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177659-56-2Relevant academic research and scientific papers

Destruxin analogues: Depsi peptidic bond replacement by amide bond

Cavelier,Jacquier,Mercadier,Verducci

, p. 6173 - 6186 (2007/10/03)

In order to determine the importance of the depsi bond present in natural destruxins, we have investigated the replacement of this ester bond by an amide bond, leading to a new family of analogues. Synthesis of six specific members of this new class of compounds is reported. Since none of these cyclopeptides showed any biological activity, we undoubtedly proved that the depside group is a requisite for insecticide effect.

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