Welcome to LookChem.com Sign In|Join Free
  • or
(R)-3,3'-DIBROMO-2,2'-DIMETHOXY-1,1'-BINAPHTHYL is a chiral binaphthyl compound characterized by the presence of two bromine atoms and two methoxy groups attached to a central binaphthyl unit. It is widely recognized for its utility as a chiral ligand and catalyst in asymmetric synthesis, particularly in the realms of organic chemistry and pharmaceutical research. (R)-3,3'-DIBROMO-2,2'-DIMETHOXY-1,1'-BINAPHTHYL's distinctive stereochemistry and three-dimensional structure render it an invaluable asset for the production of enantiomerically pure compounds, a critical aspect in the development of pharmaceuticals and fine chemicals. Furthermore, its electron-rich nature and steric properties contribute to its effectiveness as a chiral ligand in a variety of transition metal-catalyzed reactions. (R)-3,3'-DIBROMO-2,2'-DIMETHOXY-1,1'-BINAPHTHYL is instrumental in the progress of asymmetric synthesis and the generation of chiral molecules with high optical purity.

75640-69-6

Post Buying Request

75640-69-6 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

75640-69-6 Usage

Uses

Used in Pharmaceutical Research and Development:
(R)-3,3'-DIBROMO-2,2'-DIMETHOXY-1,1'-BINAPHTHYL is used as a chiral ligand and catalyst for the synthesis of enantiomerically pure compounds, which is essential in the creation of pharmaceuticals with specific biological activities. Its ability to catalyze asymmetric reactions ensures the production of desired enantiomers, contributing to the development of more effective and safer medications.
Used in Organic Chemistry:
In the field of organic chemistry, (R)-3,3'-DIBROMO-2,2'-DIMETHOXY-1,1'-BINAPHTHYL serves as a key chiral ligand and catalyst, facilitating the synthesis of complex organic molecules with high optical purity. This is particularly important in the synthesis of natural products and the development of new materials with specific properties.
Used in Asymmetric Synthesis:
(R)-3,3'-DIBROMO-2,2'-DIMETHOXY-1,1'-BINAPHTHYL is utilized as a chiral catalyst in various asymmetric reactions, enabling the selective formation of one enantiomer over another. This selective synthesis is crucial for the production of chiral molecules with high optical purity, which are often required in applications such as pharmaceuticals, agrochemicals, and fragrances.
Used in Transition Metal-Catalyzed Reactions:
As a chiral ligand, (R)-3,3'-DIBROMO-2,2'-DIMETHOXY-1,1'-BINAPHTHYL is employed in transition metal-catalyzed reactions to impart enantioselectivity and control the stereochemistry of the products. This application is vital in the synthesis of complex chiral molecules with potential applications in various industries, including pharmaceuticals, materials science, and specialty chemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 75640-69-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,6,4 and 0 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 75640-69:
(7*7)+(6*5)+(5*6)+(4*4)+(3*0)+(2*6)+(1*9)=146
146 % 10 = 6
So 75640-69-6 is a valid CAS Registry Number.

75640-69-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,3'-Dibromo-2,2'-dimethoxy-1,1'-binaphthalene

1.2 Other means of identification

Product number -
Other names (R)-3,3'-DIBROMO-1,1'-BI-2-NAPHTHOL DIMETHYL ETHER

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:75640-69-6 SDS

75640-69-6Relevant academic research and scientific papers

Oxidation of BINOLs by Hypervalent Iodine Reagents: Facile Synthesis of Xanthenes and Lactones

Wirth, Thomas,Zhang, Huaiyuan

supporting information, (2022/03/17)

Xanthene derivatives have broad applications in medicines, fluorescent probes, dyes, food additives, etc. Therefore, much attention was focused on developing the synthetic methods to prepare these compounds. Binaphthyl-based xanthene derivatives were prepared through the oxidation of BINOLs promoted by the hypervalent iodine reagent iodosylbenzene (PhIO). Nine-membered lactones were obtained through a similar oxidative reaction when iodoxybenzene (PhIO2) was used. Additionally, one-pot reactions of BINOLs, PhIO and nucleophiles such as alcohols and amines were also investigated to provide alkoxylated products and amides in good to excellent yields.

Chiral Mo-binol complexes: Activity, synthesis, and structure. Efficient enantioselective six-membered ring synthesis through catalytic metathesis

Zhu, S. Sherry,Cefalo, Dustin R.,La, Daniel S.,Jamieson, Jennifer Y.,Davis, William M.,Hoveyda, Amir H.,Schrock, Richard R.

, p. 8251 - 8259 (2007/10/03)

A new class of chiral Mo-based complexes 2a and 2b, bearing functionalized chiral binol ligands, is disclosed. Mo complex 2a promotes the asymmetric ring-closing metathesis (ARCM) of various dienes and trienes to afford six-membered carbo- and heterocycle

Host-Guest Complexation. 23. High Chiral Recognition of Amino Acid and Ester Guests by Hosts Containing One Chiral Element

Lingenfelter, David S.,Helgeson, Roger C.,Cram, Donald J.

, p. 393 - 406 (2007/10/02)

The chiral recognition properties of ten enantiomerically pure hosts toward the enantiomers of six different amino acids and their methyl esters have been examined.The hosts possessed the general structure (A)2D(OEOEO)2E, in which D is the chiral 1,1'-din

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 75640-69-6