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CS-W001157 4
Total: USD 88.00

(2S,2'S,3S,3'S)-Bis-BIDIME

  • CAS No. 1435940-21-8

  • Cat. No. CS-0088631
  • Purity≥95%
  • MDL No.MFCD31707598

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

(2S,2'S,3S,3'S)-Bis-BIDIME|CS-0088631

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General Information

  • CAS No. 1435940-21-8
  • Cat. No. CS-0088631
  • Purity ≥95%
  • MDL No. MFCD31707598
  • Storage 4°C, protect from light, stored under nitrogen
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₃₈H₄₄O₆P₂
  • Molecular Weight 658.70
  • Synonym(s) tert-butyl-4-(2,6-dimethoxyphenyl)-2,3-dihydro-1,3-benzoxaphosphol-2-yl]-4-(2,6-dimethoxyphenyl)-
  • SMILES [H][C@@]1([C@@]2([H])[P@](C(C)(C)C)C(C(C3=C(OC)C=CC=C3OC)=CC=C4)=C4O2)[P@@](C(C)(C)C)C5=C(C6=C(OC)C=CC=C6OC)C=CC=C5O1

Description

This chiral bis-bidentate ligand features two rigid, sterically defined imidazole-containing arms that enable precise metal coordination. Designed for asymmetric catalysis, it delivers high enantioselectivity in transition-metal-catalyzed transformations. The scaffold’s rigidity and defined stereochemistry enhance reproducibility and catalyst performance under standard conditions.

Application

(2S,2'S,3S,3'S)-Bis-BIDIME serves as a stereochemically defined chiral ligand scaffold for transition-metal catalysis, enabling asymmetric transformations in cross-coupling and hydrogenation reactions. Its rigid bis-bidentate architecture enhances enantioselectivity and catalyst stability, offering robust performance in synthetic workflows requiring high diastereoselectivity and operational simplicity.

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

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Computational Chemistry Data

  • TPSA   55.38
  • LogP   9.0036
  • H_Acceptors   6
  • H_Donors   0
  • Rotatable_Bonds   7

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