Cas 138517-60-9,(-)-1,2:5,6-di-O-isopropylidene-3,4-bis-O-<2'-(diphenylphosphino)benzoyl>-D-mannitol

138517-60-9

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Basic information

Product Name: (-)-1,2:5,6-di-O-isopropylidene-3,4-bis-O-<2'-(diphenylphosphino)benzoyl>-D-mannitol
Synonyms: (-)-1,2:5,6-di-O-isopropylidene-3,4-bis-O-<2'-(diphenylphosphino)benzoyl>-D-mannitol
CAS NO:138517-60-9
Molecular Formula:
Molecular Weight: 838.874
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: (-)-1,2:5,6-di-O-isopropylidene-3,4-bis-O-<2'-(diphenylphosphino)benzoyl>-D-mannitol(CAS DataBase Reference)
NIST Chemistry Reference: (-)-1,2:5,6-di-O-isopropylidene-3,4-bis-O-<2'-(diphenylphosphino)benzoyl>-D-mannitol(138517-60-9)
EPA Substance Registry System: (-)-1,2:5,6-di-O-isopropylidene-3,4-bis-O-<2'-(diphenylphosphino)benzoyl>-D-mannitol(138517-60-9)

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: 138517-60-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 138517-60-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,5,1 and 7 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 138517-60:
(8*1)+(7*3)+(6*8)+(5*5)+(4*1)+(3*7)+(2*6)+(1*0)=139
139 % 10 = 9
So 138517-60-9 is a valid CAS Registry Number.

138517-60-9Upstream product

138517-60-9Downstream Products

138517-60-9Relevant academic research and scientific papers

A modular approach for ligand design for asymmetric allylic alkylations via enantioselective palladium-catalyzed ionizations

Trost, Barry M.,Van Vranken, David L.,Bingel, Carsten

, p. 9327 - 9343 (2007/10/02)

A new class of ligands for asymmetric transition metal catalysis based on 2-(diphenylphosphino)benzoic acid was used in a mechanistically-defined palladium-catalyzed reaction in which enantiodifferentiation was the result of selective ionization of substr

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