Cas 347187-99-9,(S)-3-((S)-2-{[(S)-1-(2-Benzoylamino-acetyl)-pyrrolidine-2-carbonyl]-amino}-4-methyl-pentanoylamino)-2-tert-butoxycarbonylamino-propionic acid

347187-99-9

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Basic information

Product Name: (S)-3-((S)-2-{[(S)-1-(2-Benzoylamino-acetyl)-pyrrolidine-2-carbonyl]-amino}-4-methyl-pentanoylamino)-2-tert-butoxycarbonylamino-propionic acid
Synonyms: (S)-3-((S)-2-{[(S)-1-(2-Benzoylamino-acetyl)-pyrrolidine-2-carbonyl]-amino}-4-methyl-pentanoylamino)-2-tert-butoxycarbonylamino-propionic acid
CAS NO:347187-99-9
Molecular Formula:
Molecular Weight: 575.662
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)-3-((S)-2-{[(S)-1-(2-Benzoylamino-acetyl)-pyrrolidine-2-carbonyl]-amino}-4-methyl-pentanoylamino)-2-tert-butoxycarbonylamino-propionic acid(CAS DataBase Reference)
NIST Chemistry Reference: (S)-3-((S)-2-{[(S)-1-(2-Benzoylamino-acetyl)-pyrrolidine-2-carbonyl]-amino}-4-methyl-pentanoylamino)-2-tert-butoxycarbonylamino-propionic acid(347187-99-9)
EPA Substance Registry System: (S)-3-((S)-2-{[(S)-1-(2-Benzoylamino-acetyl)-pyrrolidine-2-carbonyl]-amino}-4-methyl-pentanoylamino)-2-tert-butoxycarbonylamino-propionic acid(347187-99-9)

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: 347187-99-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 347187-99-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,7,1,8 and 7 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 347187-99:
(8*3)+(7*4)+(6*7)+(5*1)+(4*8)+(3*7)+(2*9)+(1*9)=179
179 % 10 = 9
So 347187-99-9 is a valid CAS Registry Number.

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347187-99-9Relevant academic research and scientific papers

Design and synthesis of carboxylate inhibitors for matrix metalloproteinases

Fujisawa,Katakura,Odake,Morita,Yasuda,Yasumatsu,Morikawa

, p. 1272 - 1279 (2007/10/03)

A series of carboxylate compounds were prepared from Nα-substituted 2,3-diaminopropionic acid and were tested for efficacy as matrix metalloproteinase (MMP) inhibitors. During modeling of the initial compound 10a, we utilized three-dimensional

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