1170783-74-0

Basic information

• Product Name: (2-bromo-5-methoxyphenyl)methanaminehydrochloride
• Synonyms: (2-bromo-5-methoxyphenyl)methanaminehydrochloride;Benzenemethanamine, 2-bromo-5-methoxy-, hydrochloride (1:1)
• CAS NO: 1170783-74-0
• Molecular Formula: C₈H₁₀BrNO*ClH
• Molecular Weight: 252.53604
• Mol File: 1170783-74-0.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• Storage Temp.: Inert atmosphere,Room Temperature
• CAS DataBase Reference: (2-bromo-5-methoxyphenyl)methanaminehydrochloride(CAS DataBase Reference)
• NIST Chemistry Reference: (2-bromo-5-methoxyphenyl)methanaminehydrochloride(1170783-74-0)
• EPA Substance Registry System: (2-bromo-5-methoxyphenyl)methanaminehydrochloride(1170783-74-0)

Safety Data

• Hazardous Substances Data: 1170783-74-0(Hazardous Substances Data)

Usage

General Description

The chemical (2-bromo-5-methoxyphenyl)methanaminehydrochloride, also known as 5-Bromo-2-methoxybenzylamine hydrochloride, is a compound with the molecular formula C8H10BrNO?HCl. It is a hydrochloride salt of the amine compound, which is commonly used in organic synthesis and pharmaceutical research. The chemical features a bromo and methoxy substituent on the phenyl ring, providing unique reactivity and potential for various applications. It is known for its potential as a building block in the synthesis of biologically active compounds and pharmaceuticals, making it a valuable tool in drug discovery and development.

Upstream product

• 22921-68-2 2-bromo-5-methoxy-benzoic acid 
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Relevant articles and documents

Leuckart-Wallach Route Toward Isocyanides and Some Applications

Isocyanide-based multicomponent reactions (IMCR) are among the most important chemical reactions to efficiently generate molecular diversity and have found widespread use in industry and academia. Generally, isocyanides are synthesized in 1-2 steps starting from primary amines. Here, we provide experimental detail on an alternative approach toward formamides and, thus, isocyanides via the Leuckart-Wallach reaction in an improved variation. The resulting >50 synthesized and characterized formamides are useful starting materials for IMCR, as well as other chemistries. The advantage of using the Leuckart-Wallach pathway to formamides and isocyanides is the lower price, on average, of the starting materials, as well as their differential and complementary structural diversity, as compared to the primary amine pathway.