705931-85-7

Basic information

• Product Name: (1S)-2'-(broMoMethyl)-[1,1'-Binaphthalene]-2-carboxaldehyde
• Synonyms: (1S)-2'-(broMoMethyl)-[1,1'-Binaphthalene]-2-carboxaldehyde;(S)-2'-(Bromomethyl)-[1,1'-binaphthalene]-2-carboxaldehyde,99%e.e.;(S)-2'-(Bromomethyl)-[1,1'-binaphthalene]-2-carboxaldehyde
• CAS NO: 705931-85-7
• Molecular Formula: C22H15BrO
• Molecular Weight: 375.2579
• Mol File: 705931-85-7.mol
• Article Data: 0

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (1S)-2'-(broMoMethyl)-[1,1'-Binaphthalene]-2-carboxaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: (1S)-2'-(broMoMethyl)-[1,1'-Binaphthalene]-2-carboxaldehyde(705931-85-7)
• EPA Substance Registry System: (1S)-2'-(broMoMethyl)-[1,1'-Binaphthalene]-2-carboxaldehyde(705931-85-7)

Safety Data

• Hazardous Substances Data: 705931-85-7(Hazardous Substances Data)

Usage

Description

(1S)-2'-(bromoMethyl)-[1,1'-Binaphthalene]-2-carboxaldehyde is a chiral organic chemical compound with the molecular formula C21H15BrO. It is a derivative of binaphthalene, a hydrocarbon consisting of two naphthalene rings connected by a single bond. (1S)-2'-(broMoMethyl)-[1,1'-Binaphthalene]-2-carboxaldehyde contains a bromomethyl group attached to one of the naphthalene rings and an aldehyde group on the other, making it a functionalized derivative of binaphthalene. As a chiral compound, it exists in two enantiomeric forms, with the (1S) configuration denoting the stereochemistry of the molecule. Its unique structure and potential reactivity may contribute to various applications in organic synthesis, medicinal chemistry, or materials science.

Uses

Used in Organic Synthesis:
(1S)-2'-(bromoMethyl)-[1,1'-Binaphthalene]-2-carboxaldehyde is used as a building block for the synthesis of more complex organic molecules. Its bromomethyl and aldehyde functional groups provide opportunities for further chemical reactions, enabling the creation of a wide range of compounds with diverse properties and applications.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (1S)-2'-(bromoMethyl)-[1,1'-Binaphthalene]-2-carboxaldehyde may be utilized as a precursor for the development of pharmaceutical compounds. Its chiral nature and unique structure can be exploited to design enantioselective drugs, which can have improved efficacy and reduced side effects compared to their racemic counterparts.
Used in Materials Science:
(1S)-2'-(bromoMethyl)-[1,1'-Binaphthalene]-2-carboxaldehyde can also be employed in materials science for the development of new materials with specific properties. Its functional groups and chiral nature may contribute to the creation of materials with unique optical, electronic, or mechanical characteristics, which can be applied in various industries, such as electronics, nanotechnology, or polymer science.