91028-76-1

Usage

Uses

Used in Pharmaceutical Industry:
2-Amino-3-buten-1-ol is used as an intermediate in the synthesis of various pharmaceuticals for its ability to be incorporated into complex organic molecules.
Used in Agricultural Chemicals Industry:
2-Amino-3-buten-1-ol is used in the production of agricultural chemicals, contributing to the development of new compounds for crop protection and other agricultural applications.
Used in Organic Synthesis:
2-Amino-3-buten-1-ol is used as a reagent in organic synthesis, facilitating the creation of a wide range of organic materials.
Used in Flavors and Fragrances Industry:
2-Amino-3-buten-1-ol is used in the production of flavors and fragrances, adding to the diversity of scents and tastes in various consumer products.
Used in Medical Research:
2-Amino-3-buten-1-ol has potential applications in the field of medicine, including its exploration as a potential therapeutic agent for various diseases, due to its unique chemical properties and reactivity.

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 academic research and scientific papers

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 rare-earth element compound.

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.

PROCESS FOR PRODUCING METHIONINE

The present invention relates to a process for producing methionine, comprising a first step of reacting 2-amino-3-buten-1-ol with methanethiol, and a second step of oxidizing 2-amino-4-methylthio-1-butanol obtained in the first step. The present invention also relates to a process for producing 2-amino-4-methylthio-1-butanol, comprising a step of reacting 2-amino-3-buten-1-ol with methanethiol.