Cas 130697-38-0,Benzyl-[(R)-1-((2R,6S)-6-hydroxy-3-oxo-3,6-dihydro-2H-pyran-2-yl)-ethyl]-carbamic acid tert-butyl ester

130697-38-0

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Basic information

Product Name: Benzyl-[(R)-1-((2R,6S)-6-hydroxy-3-oxo-3,6-dihydro-2H-pyran-2-yl)-ethyl]-carbamic acid tert-butyl ester
Synonyms:
CAS NO:130697-38-0
Molecular Formula:
Molecular Weight: 347.411
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: Benzyl-[(R)-1-((2R,6S)-6-hydroxy-3-oxo-3,6-dihydro-2H-pyran-2-yl)-ethyl]-carbamic acid tert-butyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Benzyl-[(R)-1-((2R,6S)-6-hydroxy-3-oxo-3,6-dihydro-2H-pyran-2-yl)-ethyl]-carbamic acid tert-butyl ester(130697-38-0)
EPA Substance Registry System: Benzyl-[(R)-1-((2R,6S)-6-hydroxy-3-oxo-3,6-dihydro-2H-pyran-2-yl)-ethyl]-carbamic acid tert-butyl ester(130697-38-0)

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: 130697-38-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 130697-38-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,6,9 and 7 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 130697-38:
(8*1)+(7*3)+(6*0)+(5*6)+(4*9)+(3*7)+(2*3)+(1*8)=130
130 % 10 = 0
So 130697-38-0 is a valid CAS Registry Number.

130697-38-0Upstream product

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130697-38-0Relevant academic research and scientific papers

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

Raczko,Golebiowski,Krajewski,Gluzinski,Jurczak

, p. 3797 - 3800 (2007/10/02)

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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