Cas 13512-34-0,(S)-2-((S)-2-Benzyloxycarbonylamino-4-methyl-pentanoylamino)-3-(4-tert-butoxy-phenyl)-propionic acid methyl ester

13512-34-0

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Basic information

Product Name: (S)-2-((S)-2-Benzyloxycarbonylamino-4-methyl-pentanoylamino)-3-(4-tert-butoxy-phenyl)-propionic acid methyl ester
Synonyms:
CAS NO:13512-34-0
Molecular Formula:
Molecular Weight: 498.62
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-Benzyloxycarbonylamino-4-methyl-pentanoylamino)-3-(4-tert-butoxy-phenyl)-propionic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (S)-2-((S)-2-Benzyloxycarbonylamino-4-methyl-pentanoylamino)-3-(4-tert-butoxy-phenyl)-propionic acid methyl ester(13512-34-0)
EPA Substance Registry System: (S)-2-((S)-2-Benzyloxycarbonylamino-4-methyl-pentanoylamino)-3-(4-tert-butoxy-phenyl)-propionic acid methyl ester(13512-34-0)

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: 13512-34-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 13512-34-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,5,1 and 2 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 13512-34:
(7*1)+(6*3)+(5*5)+(4*1)+(3*2)+(2*3)+(1*4)=70
70 % 10 = 0
So 13512-34-0 is a valid CAS Registry Number.

13512-34-0Upstream product

13512-34-0Downstream Products

886758-84-5 {(S)-1-[(S)-2-(4-tert-Butoxy-phenyl)-1-carbamoyl-ethylcarbamoyl]-3-methyl-butyl}-carbamic acid benzyl ester

13512-34-0Relevant academic research and scientific papers

Dipeptide nitrile inhibitors of cathepsin K

Altmann, Eva,Aichholz, Reiner,Betschart, Claudia,Buhl, Thomas,Green, Jonathan,Lattmann, Rene,Missbach, Martin

, p. 2549 - 2554 (2006)

A series of dipeptidyl nitriles as inhibitors of cathepsin K have been explored starting from lead structure 1 (Cbz-Leu-NH-CH2-CN, IC 50 = 39 nM). Attachment of non-natural amino acid side chains in P1 and modification of the P3 subu

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