4828-94-8

Basic information

• Product Name: 2-(But-3-en-2-yl)aniline
• Synonyms: 2-(But-3-en-2-yl)aniline
• CAS NO: 4828-94-8
• Molecular Formula: C₁₀H₁₃N
• Molecular Weight: 147.21692
• Mol File: 4828-94-8.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 238.8±9.0 °C(Predicted)
• Appearance: /
• Density: 0.959±0.06 g/cm3(Predicted)
• Storage Temp.: 2-8°C
• PKA: 4.05±0.10(Predicted)
• CAS DataBase Reference: 2-(But-3-en-2-yl)aniline(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(But-3-en-2-yl)aniline(4828-94-8)
• EPA Substance Registry System: 2-(But-3-en-2-yl)aniline(4828-94-8)

Safety Data

• Hazardous Substances Data: 4828-94-8(Hazardous Substances Data)

Usage

General Description

2-(But-3-en-2-yl)aniline, also known as 3-buten-2-ylaniline, is an organic compound with the chemical formula C10H13N. It is classified as an aniline derivative, which is a type of aromatic amine. This chemical is commonly used in the synthesis of various pharmaceuticals, dyes, and other organic compounds due to its reactivity and functional group properties. It is an important building block in the production of organic compounds and is used in the manufacturing of various products. However, it is important to handle this chemical with care as it can be toxic and harmful if not used properly.

Upstream product

• 6246-96-4 N-(2-buten-1-yl)aniline 
• 69611-44-5 N-(3-methyl-2-butyne)aniline 
• 62722-94-5 (Z)-N-(but-2-en-1-yl)aniline 
• 114067-35-5 ((E)-2-butenyl)trifluorosilane 
• 615-43-0 2-iodophenylamine 
• 62-53-3 aniline 

Downstream Products

• 1211480-94-2 N-allyl-2-(but-3-en-2-yl)aniline 
• 1597592-81-8 N-(2-bromobenzyl)-2-(but-3-en-2-yl)aniline 
• 1441228-30-3 1-azido-2-(but-3-en-2-yl)benzene 
• 1326627-32-0 C₁₃H₁₅NO 
• 41652-87-3 (+/-)-N,N-dimethyl-2-(1'-methylallyl)aniline 

Relevant articles and documents

Palladium-Catalyzed Dehydrogenative Difunctionalization of Aminoalkenes with Aminals as Oxidants and Electrophiles

A novel palladium-catalyzed aminomethylamination of aminoalkenes with an aminal, functioning not only as an aminomethylation reagent but also as an oxidant, was developed. This direct and operationally simple protocol provides a fundamentally novel and unique approach toward the synthesis of 2-(2-aminoethyl)indoles and 2-(2-aminoethyl)pyrrolidines, which are important building blocks in synthetic organic chemistry. The unity of this method was highlighted by the rapid synthesis of Alosetron, a drug used for the treatment of irritable bowel syndrome.

Palladium(II)-catalyzed oxidative cascade cyclization reactions of anilides and anilines: Scope and mechanistic investigations

With Pd(OAc)2/pyridine as the catalyst system and molecular oxygen as a green oxidant, acrylanilides and N-allylanilines undergo oxidative cascade cyclization to form heterocyclic rings in high yields. This methodology is applicable to acrylani

γ-Selective Cross-Coupling Reactions of Allyltrifluorosilanes: A New Approach to Regiochemical Control in Allylic Systems

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