Cas 255052-80-3,((1S,2S,3S,4S)-1-Benzyl-4-carbamoyl-2,3-dihydroxy-5-methyl-hexyl)-carbamic acid tert-butyl ester

255052-80-3

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Basic information

Product Name: ((1S,2S,3S,4S)-1-Benzyl-4-carbamoyl-2,3-dihydroxy-5-methyl-hexyl)-carbamic acid tert-butyl ester
Synonyms:
CAS NO:255052-80-3
Molecular Formula:
Molecular Weight: 380.484
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: ((1S,2S,3S,4S)-1-Benzyl-4-carbamoyl-2,3-dihydroxy-5-methyl-hexyl)-carbamic acid tert-butyl ester(CAS DataBase Reference)
NIST Chemistry Reference: ((1S,2S,3S,4S)-1-Benzyl-4-carbamoyl-2,3-dihydroxy-5-methyl-hexyl)-carbamic acid tert-butyl ester(255052-80-3)
EPA Substance Registry System: ((1S,2S,3S,4S)-1-Benzyl-4-carbamoyl-2,3-dihydroxy-5-methyl-hexyl)-carbamic acid tert-butyl ester(255052-80-3)

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: 255052-80-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 255052-80-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,5,0,5 and 2 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 255052-80:
(8*2)+(7*5)+(6*5)+(5*0)+(4*5)+(3*2)+(2*8)+(1*0)=123
123 % 10 = 3
So 255052-80-3 is a valid CAS Registry Number.

255052-80-3Upstream product

255052-76-7 ((1S,2S,3S,4R)-1-Benzyl-4-cyano-2,3-dihydroxy-5-methyl-hexyl)-carbamic acid tert-butyl ester

255052-80-3Downstream Products

255052-80-3Relevant academic research and scientific papers

Stereoselective synthesis of non symmetric dihydroxyethylene dipeptide isosteres via epoxyalcohols derived from α-amino acids

Benedetti, Fabio,Magnan, Monica,Miertus, Stanislav,Norbedo, Stefano,Parat, Djiana,Tossi, Alessandro

, p. 3027 - 3030 (2007/10/03)

(1R,2R,3S,4S)-4-Amino-3-hydroxy-1,2-epoxybutanes, accessible in four steps from L-aminoesters, react regio- and stereoselectively with diethyl aluminum cyanide to give (1R,2S,3S,4S)-4-amino-2,3-dihydroxynitriles. Hydrolysis yields hydroxylactones equivale

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