Cas 130628-84-1,[(R)-1-(6-Hydroxy-3-oxo-3,6-dihydro-2H-pyran-2-yl)-ethyl]-methyl-carbamic acid tert-butyl ester

130628-84-1

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Basic information

Product Name: [(R)-1-(6-Hydroxy-3-oxo-3,6-dihydro-2H-pyran-2-yl)-ethyl]-methyl-carbamic acid tert-butyl ester
Synonyms:
CAS NO:130628-84-1
Molecular Formula:
Molecular Weight: 271.313
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: [(R)-1-(6-Hydroxy-3-oxo-3,6-dihydro-2H-pyran-2-yl)-ethyl]-methyl-carbamic acid tert-butyl ester(CAS DataBase Reference)
NIST Chemistry Reference: [(R)-1-(6-Hydroxy-3-oxo-3,6-dihydro-2H-pyran-2-yl)-ethyl]-methyl-carbamic acid tert-butyl ester(130628-84-1)
EPA Substance Registry System: [(R)-1-(6-Hydroxy-3-oxo-3,6-dihydro-2H-pyran-2-yl)-ethyl]-methyl-carbamic acid tert-butyl ester(130628-84-1)

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: 130628-84-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 130628-84-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,6,2 and 8 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 130628-84:
(8*1)+(7*3)+(6*0)+(5*6)+(4*2)+(3*8)+(2*8)+(1*4)=111
111 % 10 = 1
So 130628-84-1 is a valid CAS Registry Number.

130628-84-1Upstream product

130628-78-3 ((R)-2-Furan-2-yl-2-hydroxy-1-methyl-ethyl)-methyl-carbamic acid tert-butyl ester

130628-84-1Downstream Products

130628-84-1Relevant academic research and scientific papers

Stereoselective addition of furyllithium to variously N,N-diprotected D-alaninals

Raczko,Golebiowski,Krajewski,Gluzinski,Jurczak

, p. 3797 - 3800 (1990)

A highly stereoselective route to derivatives of 2-amino-1-(2'-furyl)-propan-1-ol via addition of furyllithium to variously N,N-diprotected D-alaninals is described. An efficient conversion of these compounds into aminosugar precursors - chiral uloses is

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