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CS-W001157 4
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(R)-3-(tert-Butyl)-4-(3,5-diisopropyl-2,6-dimethoxyphenyl)-2,3-dihydrobenzo[d][1,3]oxaphosphole

  • CAS No. 2351219-90-2

  • Cat. No. CS-0092211
  • Purity≥97%
  • MDL No.MFCD32641161

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

(R)-3-(tert-Butyl)-4-(3,5-diisopropyl-2,6-dimethoxyphenyl)-2,3-dihydrobenzo[d][1,3]oxaphosphole|CS-0092211

Structure of 2351219-90-2

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General Information

  • CAS No. 2351219-90-2
  • Cat. No. CS-0092211
  • Purity ≥97%
  • MDL No. MFCD32641161
  • Storage 4°C, protect from light, stored under nitrogen
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₂₅H₃₅O₃P
  • Molecular Weight 414.52
  • Synonym(s) None
  • SMILES COC1=C(C(C)C)C=C(C(C)C)C(OC)=C1C2=C([P@@](C(C)(C)C)CO3)C3=CC=C2

Description

This chiral phosphole features a sterically shielded tert-butyl group and an electron-rich aryl moiety with dual methoxy and isopropyl substituents, enabling robust coordination in asymmetric catalysis. Its bench-stable, moisture-tolerant structure simplifies handling in air-sensitive transformations.

Application

(R)-3-(tert-Butyl)-4-(3,5-diisopropyl-2,6-dimethoxyphenyl)-2,3-dihydrobenzo[d][1,3]oxaphosphole serves as a sterically encumbered, bench-stable phosphole scaffold enabling efficient transition-metal-catalyzed cross-coupling reactions. Its ortho-dimethoxy substitution enhances electronic modulation and solubility, while the chiral tertiary phosphorus center provides stereochemical control in asymmetric synthesis. Functions effectively in Pd-catalyzed coupling protocols and acts as a versatile building block for 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   6.8732
  • H_Acceptors   3
  • H_Donors   0
  • Rotatable_Bonds   5

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