671-56-7

Usage

Uses

Used in Organic Synthesis:
1-chloro-2-hydroxy-3-butene is used as a chemical intermediate for the synthesis of various compounds, leveraging its reactive nature to facilitate the formation of new chemical entities.
Used in Pharmaceutical Industry:
1-chloro-2-hydroxy-3-butene is utilized as a building block in the development of pharmaceuticals, contributing to the creation of novel drug molecules with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, 1-chloro-2-hydroxy-3-butene serves as a key intermediate in the synthesis of agrochemicals, such as pesticides and herbicides, to enhance crop protection and yield.
Given the compound's reactivity and potential applications across different industries, it is essential to handle 1-chloro-2-hydroxy-3-butene with care to mitigate any associated risks.

InChI:InChI=1/C4H7ClO/c1-2-4(6)3-5/h2,4,6H,1,3H2

Upstream product

• 507-40-4 tert-butylhypochlorite 
• 67-66-3 chloroform 
• 64-19-7 acetic acid 
• 106-99-0 buta-1,3-diene 
• 3135-74-8 chlorourea 
• 64-18-6 formic acid 
• 7732-18-5 water 
• 13898-47-0 hypochloric acid 

Downstream Products

• 7268-35-1 meso-1,4-dichlorobutane-2,3-diol 
• 13635-05-7 3-hydroxyvaleronitrile 
• 7451-41-4 3-[1]naphthylcarbamoyloxy-pent-4-enenitrile 
• 930-22-3 epoxybutene 
• 17687-76-2 erythrol-1-methyl ether 
• 497-06-3 3,4-butenediol 
• 1873-25-2 1-chloro-butan-2-ol 
• 2651-83-4 1,3,4-trichloro-butan-2-ol 
• 64248-98-2 2,4-dichloro-butane-1,3-diol 
• 3141-84-2 1-diethylamino-but-3-en-2-ol 
• 90326-08-2 phosphorous acid 1-chloromethyl-allyl ester diethyl ester 
• 17864-75-4 Bis-(1-chlormethyl-propen-⁽²⁾-yloxy)-methyl-silan 
• 821-11-4 trans-butene-1,4-diol 
• 25476-89-5 1-chloro-3-buten-2-one 

Relevant academic research and scientific papers

Alkylation of 5-Substituted Tetrazoles with Various Alcohols in 1,2-Dichloroethane in the Presence of BF3·Et2O

Abstract: The alkylation of 1H-tetrazole, 5-methyl-1H-tetrazole, and 5-phenyl-1H-tetrazole with primary, secondary, and tertiary alcohols, including benzylic and allylic ones, have been studied in 1,2-dichloroethane in the presence of boron trifluoride–diethyl ether complex. Neither primary nor secondary saturated alcohols alkylated tetrazoles in the given system. Tertiary alcohols such tert-butyl alcohol and adamantan-1-ol reacted with unsubstituted and 5-substituted tetrazoles to give 70–85% of the corresponding 2-alkyl-5-R-tetrazoles with high regioselectivity. The alkylation of 1H-tetrazole with benzyl alcohol afforded 55% of 2-benzyl-2H-tetrazole as the only product. The alkylation of 1H-tetrazole with various allylic alcohols led to the formation of mixtures of 2-alkyl-2H-tetrazoles with isomeric alkyl substituents.

Synthesis of 2-Hydroxybut-3-enylglucosinolate (Progoitrin)

A synthesis of 2-hydroxybut-3-enylglucosinolate (progoitrin) is described.Its properties and authentication of its biological activity are discussed.This is the first time that this particular glucosinolate has been isolated in pure form by synthesis.