29158-40-5

Basic information

• Product Name: sodium boron(-1) anion
• Synonyms: sodium boron(-1) anion
• CAS NO: 29158-40-5
• Molecular Formula: BNa
• Molecular Weight: 33.80077
• Mol File: 29158-40-5.mol
• Article Data: 0

Chemical Properties

• Appearance: /
• CAS DataBase Reference: sodium boron(-1) anion(CAS DataBase Reference)
• NIST Chemistry Reference: sodium boron(-1) anion(29158-40-5)
• EPA Substance Registry System: sodium boron(-1) anion(29158-40-5)

Safety Data

• Hazardous Substances Data: 29158-40-5(Hazardous Substances Data)

Usage

Description

Sodium boron(-1) anion, a chemical compound composed of sodium and boron ions, is characterized by the boron ion bearing a formal negative charge. It is typically generated through the reaction of sodium borohydride with an acid, resulting in the formation of this anion. Known for its reducing properties, the sodium boron(-1) anion is adept at transferring hydride ions to various organic substrates, which makes it a versatile and valuable reagent in the realm of organic synthesis.

Uses

Used in Organic Synthesis:
Sodium boron(-1) anion is utilized as a reducing agent for the conversion of carbonyl compounds to alcohols. Its ability to selectively reduce functional groups such as nitro, nitrile, and aromatic groups makes it an indispensable tool in the synthesis of pharmaceuticals, fine chemicals, and other organic compounds.
Used in Pharmaceutical Synthesis:
In the pharmaceutical industry, the sodium boron(-1) anion is employed as a key reagent for the reduction of specific functional groups within complex organic molecules. This selective reduction capability is crucial for the production of active pharmaceutical ingredients with desired properties and minimal side effects.
Used in Fine Chemicals Production:
Sodium boron(-1) anion plays a significant role in the fine chemicals sector, where its selective reduction properties are harnessed to produce high-purity compounds with specific functionalities. This is particularly important in applications requiring high levels of selectivity and specificity, such as in the synthesis of fragrances, dyes, and other specialty chemicals.