Cas 1026554-93-7,(2S,3S)-2-Benzyloxy-N-((S)-1-benzyloxycarbonyl-2-carbamoyl-ethyl)-3-hydroxy-succinamic acid methyl ester

1026554-93-7

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Basic information

Product Name: (2S,3S)-2-Benzyloxy-N-((S)-1-benzyloxycarbonyl-2-carbamoyl-ethyl)-3-hydroxy-succinamic acid methyl ester
Synonyms:
CAS NO:1026554-93-7
Molecular Formula:
Molecular Weight: 458.468
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: (2S,3S)-2-Benzyloxy-N-((S)-1-benzyloxycarbonyl-2-carbamoyl-ethyl)-3-hydroxy-succinamic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (2S,3S)-2-Benzyloxy-N-((S)-1-benzyloxycarbonyl-2-carbamoyl-ethyl)-3-hydroxy-succinamic acid methyl ester(1026554-93-7)
EPA Substance Registry System: (2S,3S)-2-Benzyloxy-N-((S)-1-benzyloxycarbonyl-2-carbamoyl-ethyl)-3-hydroxy-succinamic acid methyl ester(1026554-93-7)

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: 1026554-93-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1026554-93-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,6,5,5 and 4 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1026554-93:
(9*1)+(8*0)+(7*2)+(6*6)+(5*5)+(4*5)+(3*4)+(2*9)+(1*3)=137
137 % 10 = 7
So 1026554-93-7 is a valid CAS Registry Number.

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1026554-93-7Relevant academic research and scientific papers

Synthesis and activity of pseudotripeptide inhibitors of HIV-1 protease containing D(-)-O-(benzyl)-tartaric acid

Marastoni, Mauro,Fantin, Giancarlo,Bortolotti, Fabrizio,Tomatis, Roberto

, p. 1099 - 1101 (2007/10/03)

Four HIV-1 protease inhibitors containing [(S,S)-O-(benzyl) tartaric acid]-Pro as a transition-state mimic were prepared and evaluated by a spectrophotometric assay. Two pseudotripeptide derivatives showed weak inhibitory activity similar to acetylpepstatin.

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