Cas 288089-63-4,(S)-4-tert-butyl-2-(2-(dicyclohexylphosphino)phenyl)-4,5-dihydrooxazole

288089-63-4

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Basic information

Product Name: (S)-4-tert-butyl-2-(2-(dicyclohexylphosphino)phenyl)-4,5-dihydrooxazole
Synonyms: (S)-4-tert-butyl-2-(2-(dicyclohexylphosphino)phenyl)-4,5-dihydrooxazole
CAS NO:288089-63-4
Molecular Formula:
Molecular Weight: 399.557
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: (S)-4-tert-butyl-2-(2-(dicyclohexylphosphino)phenyl)-4,5-dihydrooxazole(CAS DataBase Reference)
NIST Chemistry Reference: (S)-4-tert-butyl-2-(2-(dicyclohexylphosphino)phenyl)-4,5-dihydrooxazole(288089-63-4)
EPA Substance Registry System: (S)-4-tert-butyl-2-(2-(dicyclohexylphosphino)phenyl)-4,5-dihydrooxazole(288089-63-4)

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: 288089-63-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 288089-63-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,8,8,0,8 and 9 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 288089-63:
(8*2)+(7*8)+(6*8)+(5*0)+(4*8)+(3*9)+(2*6)+(1*3)=194
194 % 10 = 4
So 288089-63-4 is a valid CAS Registry Number.

288089-63-4Upstream product

154701-60-7 2-(2-bromophenyl)-4-(1,1-dimethylethyl)-4,5-dihydro-(4S)-oxazole

288089-63-4Downstream Products

288089-63-4Relevant academic research and scientific papers

A facile and modular synthesis of phosphinooxazoline ligands

Tani, Kousuke,Behenna, Douglas C.,McFadden, Ryan M.,Stoltz, Brian M.

, p. 2529 - 2531 (2007)

The copper(I) iodide catalyzed phosphine/aryl halide coupling procedure of Buchwald et al. provides modular, robust, and scaleable access to phosphinooxazoline (PHOX) ligands. The advantages of this method are highlighted by the convenient synthesis of PH

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