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(R)-3-(tert-Butyl)-4-(2,6-diphenoxyphenyl)-2,3-dihydrobenzo[d][1,3]oxaphosphole

  • CAS No. 1441830-74-5

  • Cat. No. CS-0091066
  • Molecule weight454.50
  • Purity≥97%
  • MDL No.MFCD32641149

*For research and further manufacturing use only, not for direct human use.

(R)-3-(tert-Butyl)-4-(2,6-diphenoxyphenyl)-2,3-dihydrobenzo[d][1,3]oxaphosphole|CS-0091066

Structure of 1441830-74-5

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General Information

  • CAS No. 1441830-74-5
  • Cat. No. CS-0091066
  • Purity ≥97%
  • MDL No. MFCD32641149
  • Storage 4°C, protect from light, stored under nitrogen
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₂₉H₂₇O₃P
  • Molecular Weight 454.50
  • Synonym(s) 6-diphenoxyphenyl)-2
  • SMILES CC(C)(C)[P@@]1C2=C(C3=C(OC4=CC=CC=C4)C=CC=C3OC5=CC=CC=C5)C=CC=C2OC1

Description

(R)-3-(tert-Butyl)-4-(2,6-diphenoxyphenyl)-2,3-dihydrobenzo[d][1,3]oxaphosphole is a chiral phosphole derivative featuring a sterically shielded tert-butyl group and electron-rich diphenoxy substitution. This configuration enhances stability and directs stereoselective transformations in asymmetric catalysis. The fused oxaphosphole core provides a rigid, electron-deficient platform for metal coordination, enabling efficient ligand integration in transition-metal-catalyzed processes.

Application

(R)-3-(tert-Butyl)-4-(2,6-diphenoxyphenyl)-2,3-dihydrobenzo[d][1,3]oxaphosphole serves as a stereochemically defined phosphole scaffold with enhanced bench stability and functional group tolerance. It enables efficient access to chiral phosphorus-containing building blocks via P–C bond formation, facilitates transition-metal-catalyzed coupling reactions, and functions as a versatile intermediate in the synthesis of phosphine ligands and bioactive heterocyclic systems.

Safety Information

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GHS Pictogram :
GHS No : GHS07
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H302-H315-H319-H335
Precautionary Statements : P261-P280-P302+P352

Quality Control

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Computational Chemistry Data

  • TPSA   27.69
  • LogP   8.1938
  • H_Acceptors   3
  • H_Donors   0
  • Rotatable_Bonds   5

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