Cas 850589-10-5,1,2-O-isopropylidene-3-diphenylphosphinite-5-methylsulfanyl-D-xylofuranose

850589-10-5

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Basic information

Product Name: 1,2-O-isopropylidene-3-diphenylphosphinite-5-methylsulfanyl-D-xylofuranose
Synonyms: 1,2-O-isopropylidene-3-diphenylphosphinite-5-methylsulfanyl-D-xylofuranose
CAS NO:850589-10-5
Molecular Formula:
Molecular Weight: 404.467
EINECS: N/A
Product Categories: N/A
Mol File: 850589-10-5.mol
Article Data: 2

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: 1,2-O-isopropylidene-3-diphenylphosphinite-5-methylsulfanyl-D-xylofuranose(CAS DataBase Reference)
NIST Chemistry Reference: 1,2-O-isopropylidene-3-diphenylphosphinite-5-methylsulfanyl-D-xylofuranose(850589-10-5)
EPA Substance Registry System: 1,2-O-isopropylidene-3-diphenylphosphinite-5-methylsulfanyl-D-xylofuranose(850589-10-5)

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: 850589-10-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 850589-10-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,0,5,8 and 9 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 850589-10:
(8*8)+(7*5)+(6*0)+(5*5)+(4*8)+(3*9)+(2*1)+(1*0)=185
185 % 10 = 5
So 850589-10-5 is a valid CAS Registry Number.

850589-10-5Upstream product

850589-10-5Downstream Products

850589-10-5Relevant articles and documents

Furanoside thioether-phosphinite ligands for Pd-catalyzed asymmetric allylic substitution reactions

Guimet, Eugeni,Dieguez, Montserrat,Ruiz, Aurora,Claver, Carmen

, p. 959 - 963 (2005)

A new series of thioether-phosphinite ligands, easily prepared in a few steps from inexpensive d-(+)-xylose, was tested in the Pd-catalyzed allylic substitution of substrates with different steric properties. The results show that the enantiomeric excesse

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