91028-76-1

Basic information

• Product Name: 2-Amino-3-buten-1-ol
• Synonyms: 2-Amino-3-buten-1-ol;3-Buten-1-ol, 2-aMino-;2-AMINOBUT-3-EN-1-OL
• CAS NO: 91028-76-1
• Molecular Formula: C₄H₉NO
• Molecular Weight: 87.12036
• Mol File: 91028-76-1.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 81-82 °C(Press: 14 Torr)
• Appearance: /
• Density: 0.955±0.06 g/cm3(Predicted)
• PKA: 12.54±0.10(Predicted)
• CAS DataBase Reference: 2-Amino-3-buten-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Amino-3-buten-1-ol(91028-76-1)
• EPA Substance Registry System: 2-Amino-3-buten-1-ol(91028-76-1)

Safety Data

• Hazardous Substances Data: 91028-76-1(Hazardous Substances Data)

Usage

General Description

2-Amino-3-buten-1-ol, also known as 2-aminoally l alcohol, is a chemical compound with the molecular formula C4H9NO. It is an unsaturated amino alcohol that is commonly used as an intermediate in the synthesis of various pharmaceuticals and fine chemicals. It is a colorless liquid with a strong odor, and it is soluble in water, alcohols, and other organic solvents. 2-Amino-3-buten-1-ol is primarily used in the production of pharmaceuticals, agricultural chemicals, and other organic materials. It is also used as a reagent in organic synthesis and in the production of flavors and fragrances. The compound has been found to have potential applications in the field of medicine, including as a potential therapeutic agent for various diseases.

Upstream product

• 930-22-3 epoxybutene 
• 7664-41-7 ammonia 

Downstream Products

• 96-20-8 2-aminobutanol 
• 132286-53-4 Benzoic acid 2-[((E)-4-acetoxy-3-methyl-but-2-enyl)-benzoyl-amino]-but-3-enyl ester 
• 132302-79-5 Benzoic acid 2-[((E)-4-acetoxy-but-2-enyl)-benzoyl-amino]-but-3-enyl ester 

Relevant articles and documents

PROCESS FOR PRODUCING 2 - AMINO - 3 - BUTENE - 1 - OL

The present invention provides a novel process for producing 2-amino-3-butene-1-ol compound. A process for producing 2-amino-3-butene-1-ol compound of the following formula (2) comprising a step of reacting an alkenylimide compound of the formula (3) with an ammonia. wherein R1, R2 and R3 each independently represent an alkyl group optionally having a substituent, an aryl group optionally having a substituent or a hydrogen atom; R4 and R5 each independently represent an alkyl group optionally having a substituent, an aryl group optionally having a substituent or a hydrogen atom or alternatively R4 and R5 are combined each other together with the carbon atoms to which R4 and R5 are each binded to form a cycloalkyl ring or an aromatic ring; a dashed line represents that said sites may be a double bond.

METHOD FOR PRODUCING AMINO ALCOHOL COMPOUND

Provided is a novel method that can produce an amino alcohol compound (2). A method for producing an amino alcohol compound represented by the formula (2): wherein R1, R2, and R3 each independently represent an alkyl group optionally having a substituent, an aryl group optionally having a substituent, or a hydrogen atom, the method including a step of reacting a compound represented by the formula (1): wherein R1, R2, and R3 each have the same meaning as defined above, with ammonia in the presence of a compound of Group 6 element in the periodic table.