Cas 898529-40-3,methyl (R)-2-O-(4-nitrobenzoyl)-4-(9H-fluoren-9-ylmethoxycarbonylamino)-2-hydroxybutyrate

898529-40-3

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Basic information

Product Name: methyl (R)-2-O-(4-nitrobenzoyl)-4-(9H-fluoren-9-ylmethoxycarbonylamino)-2-hydroxybutyrate
Synonyms: methyl (R)-2-O-(4-nitrobenzoyl)-4-(9H-fluoren-9-ylmethoxycarbonylamino)-2-hydroxybutyrate
CAS NO:898529-40-3
Molecular Formula:
Molecular Weight: 504.496
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: methyl (R)-2-O-(4-nitrobenzoyl)-4-(9H-fluoren-9-ylmethoxycarbonylamino)-2-hydroxybutyrate(CAS DataBase Reference)
NIST Chemistry Reference: methyl (R)-2-O-(4-nitrobenzoyl)-4-(9H-fluoren-9-ylmethoxycarbonylamino)-2-hydroxybutyrate(898529-40-3)
EPA Substance Registry System: methyl (R)-2-O-(4-nitrobenzoyl)-4-(9H-fluoren-9-ylmethoxycarbonylamino)-2-hydroxybutyrate(898529-40-3)

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: 898529-40-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 898529-40-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,8,5,2 and 9 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 898529-40:
(8*8)+(7*9)+(6*8)+(5*5)+(4*2)+(3*9)+(2*4)+(1*0)=243
243 % 10 = 3
So 898529-40-3 is a valid CAS Registry Number.

898529-40-3Upstream product

898529-40-3Downstream Products

898529-40-3Relevant academic research and scientific papers

Synthesis of arginine-containing hydroxamate dipeptidomimetics

Seo, Jiwon,Silverman, Richard B.

, p. 4069 - 4073 (2006)

The syntheses of arginine-containing hydroxamates using various peptide coupling methods are described. Fmoc-Arg(NO2)-Cl prepared at low temperature did not undergo intramolecular δ-lactam formation and effectively provided desired hydroxamates

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