Cas 1429753-22-9,tert-butyl (1-((2-(((1-((2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-2-oxo-1,2-dihydropyrimidin-4-yl)thio)selanyl)ethyl)amino)-1-oxo-3-phenylpropan-2-yl)carbamate

1429753-22-9

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Basic information

Product Name: tert-butyl (1-((2-(((1-((2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-2-oxo-1,2-dihydropyrimidin-4-yl)thio)selanyl)ethyl)amino)-1-oxo-3-phenylpropan-2-yl)carbamate
Synonyms:
CAS NO:1429753-22-9
Molecular Formula:
Molecular Weight: 629.593
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: tert-butyl (1-((2-(((1-((2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-2-oxo-1,2-dihydropyrimidin-4-yl)thio)selanyl)ethyl)amino)-1-oxo-3-phenylpropan-2-yl)carbamate(CAS DataBase Reference)
NIST Chemistry Reference: tert-butyl (1-((2-(((1-((2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-2-oxo-1,2-dihydropyrimidin-4-yl)thio)selanyl)ethyl)amino)-1-oxo-3-phenylpropan-2-yl)carbamate(1429753-22-9)
EPA Substance Registry System: tert-butyl (1-((2-(((1-((2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-2-oxo-1,2-dihydropyrimidin-4-yl)thio)selanyl)ethyl)amino)-1-oxo-3-phenylpropan-2-yl)carbamate(1429753-22-9)

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: 1429753-22-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1429753-22-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,9,7,5 and 3 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1429753-22:
(9*1)+(8*4)+(7*2)+(6*9)+(5*7)+(4*5)+(3*3)+(2*2)+(1*2)=179
179 % 10 = 9
So 1429753-22-9 is a valid CAS Registry Number.

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1429753-22-9Relevant academic research and scientific papers

Biohybrid-Se-S-coupling reactions of an amino acid derived seleninate

Abdo, Mohannad,Sun, Zhexun,Knapp, Spencer

, p. 1963 - 1972 (2013/04/24)

We describe the synthesis of the N-(2-seleninatoethyl) amide of N-Bocphenylalanine, serving here as a peptide model, and its reductive coupling reactions under mild conditions with unprotected thiouridine and glutathione. Selenosulfide products such as these comprise reversibly conjugated bio-components, and can potentially find uses as probes of biological function, such as enzyme inhibitors, delivery systems, or structural mimics.

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