(S) -BINAP

• Description:

  (S) -BINAP is the S-isomer of BINAP (HY-Y0003) . BINAP is a chiral bisphosphine ligand. (S) -BINAP can be used to assist in the synthesis of compounds with anticancer activity[1][2][3].

• UNSPSC:

  12352005

• Hazard Statement:

  H302, H315, H319, H335

• Target:

  Biochemical Assay Reagents

• Type:

  Reference compound

• Related Pathways:

  Others

• Field of Research:

  Cancer

• Assay Protocol:

  https://www.medchemexpress.com/s-binap.html

• Purity:

  99.71

• Solubility:

  DMSO : 2 mg/mL (ultrasonic; warming; heat to 60°C)

• Smiles:

  C1(C=CC=C2)=C2[C@@]([C@@]3=C(C=CC=C4)C4=CC=C3P(C5=CC=CC=C5)C6=CC=CC=C6)=C(P(C7=CC=CC=C7)C8=CC=CC=C8)C=C1

• Molecular Formula:

  C44H32P2

• Molecular Weight:

  622.67

• Precautions:

  H302, H315, H319, H335

• References & Citations:

  [1]Tunik S P, et al. Reaction of (S) -BINAP with H4Ru4 (CO) 12. The First Example of Face-Bridging BINAP Coordination and 100% Stereoselectivity in Formation of a Chiral Tetranuclear Cluster Framework. Organometallics, 2004, 23 (3) : 568-579.|[2]Li M, et al. Stereoselective Total Synthesis of Formosanol, Tsugacetal, and Methyl β-Conidendral. Org Lett. 2022 Oct 28;24 (42) :7812-7816.|[3]Xin Jin, et al. Synthesis and characterization of a high-purity chiral 5,5'-disulfonato-BINAP ligand and its application in asymmetric hydrogenation of β-keto esters. Molecular Catalysis, 2021, 507, 111562.

• Shipping Conditions:

  Room Temperature

• Storage Conditions:

  4°C (Powder, stored under nitrogen)

• Scientific Category:

  Reference compound1

• Clinical Information:

  No Development Reported

• CAS Number:

  [76189-56-5]