Cas 138517-58-5,(-)-3-aza-3-benzyl-1(R),5(R)-dihydroxy-1,5-bis-O-<2'-(diphenylphosphino)benzoyl>-1,5-diphenylpentane

138517-58-5

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Basic information

Product Name: (-)-3-aza-3-benzyl-1(R),5(R)-dihydroxy-1,5-bis-O-<2'-(diphenylphosphino)benzoyl>-1,5-diphenylpentane
Synonyms: (-)-3-aza-3-benzyl-1(R),5(R)-dihydroxy-1,5-bis-O-<2'-(diphenylphosphino)benzoyl>-1,5-diphenylpentane
CAS NO:138517-58-5
Molecular Formula:
Molecular Weight: 924.028
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: (-)-3-aza-3-benzyl-1(R),5(R)-dihydroxy-1,5-bis-O-<2'-(diphenylphosphino)benzoyl>-1,5-diphenylpentane(CAS DataBase Reference)
NIST Chemistry Reference: (-)-3-aza-3-benzyl-1(R),5(R)-dihydroxy-1,5-bis-O-<2'-(diphenylphosphino)benzoyl>-1,5-diphenylpentane(138517-58-5)
EPA Substance Registry System: (-)-3-aza-3-benzyl-1(R),5(R)-dihydroxy-1,5-bis-O-<2'-(diphenylphosphino)benzoyl>-1,5-diphenylpentane(138517-58-5)

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: 138517-58-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 138517-58-5 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, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 138517-58:
(8*1)+(7*3)+(6*8)+(5*5)+(4*1)+(3*7)+(2*5)+(1*8)=145
145 % 10 = 5
So 138517-58-5 is a valid CAS Registry Number.

138517-58-5Upstream product

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138517-58-5Relevant 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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