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Ethyl 2-hydroxy-2-methyl-but-3-enoate, also known as Ethyl Vinyllactate, is an organic compound that serves as an intermediate in the synthesis of various chemical compounds. It is characterized by its ester functional group and a vinyl group, which makes it a versatile building block in organic synthesis.

50471-46-0

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50471-46-0 Usage

Uses

Used in Agricultural Industry:
Ethyl 2-hydroxy-2-methyl-but-3-enoate is used as an intermediate in the synthesis of Vinclozolin (V314050), which is an agricultural fungicide. Vinclozolin is effective in controlling a wide range of fungal diseases in various crops, thereby protecting them from yield losses and ensuring food security.
In the synthesis of Vinclozolin, Ethyl Vinyllactate plays a crucial role as a precursor, contributing to the development of this important fungicide. Its presence in the synthesis process highlights the significance of Ethyl Vinyllactate in the agricultural industry, where it helps in the production of effective and widely used crop protection agents.

Check Digit Verification of cas no

The CAS Registry Mumber 50471-46-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,4,7 and 1 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 50471-46:
(7*5)+(6*0)+(5*4)+(4*7)+(3*1)+(2*4)+(1*6)=100
100 % 10 = 0
So 50471-46-0 is a valid CAS Registry Number.

50471-46-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-hydroxy-2-methylbut-3-enoate

1.2 Other means of identification

Product number -
Other names ethyl vinyl-lactate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:50471-46-0 SDS

50471-46-0Relevant academic research and scientific papers

4 - Halogenated -2 - methyl -2 - butenoic acid ethyl ester and preparation method thereof

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Paragraph 0085-0087; 0089-0126, (2021/10/20)

The invention discloses 4 - halogenated -2 - methyl -2 - butenoic acid ethyl ester and a preparation method thereof, and particularly relates to the technical field of chemical intermediate synthesis. The 4 -halogenated -2 -methyl -2 - butenoic acid ethyl ester comprises the following steps: 2 - methyl -3 - butenoic acid ethyl ester is oxidized to synthesize 2 - methyl -2 -hydroxy -3 -butenoic acid ethyl ester. The 2 -methyl -2 -hydroxy -3 -butenoic acid ethyl ester is halogenated to give 4 -halo -2 - methyl -2 -butenoic acid ethyl ester. The synthesis method is simple, the yield is high, the use of toxic liquid bromine and hydrocyanic acid is avoided, and industrial production is easy.

4-halo-2-methyl-2-butenoic acid ethyl ester preparation method

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Paragraph 0037; 0038; 0039, (2016/11/24)

The invention discloses a 4-halogenated-2-methyl-2-ethyl crotonate preparing method which includes following steps: (1) performing a Grignard reaction to ethyl pyruvate (II) and a vinyl magnesium halide Grignard reagent (III) to obtain a condensation compound (IV) after the reaction finished, and carrying out a hydrolysis reaction to the condensation compound (IV) to obtain a hydroxyl compound (V); and (2) performing a halogenating reaction to the hydroxyl compound and a haloid acid to obtain the 4-halogenated-2-methyl-2-ethyl crotonate (I). The 4-halogenated-2-methyl-2-ethyl crotonate preparing method is simple in total technology, allows raw materials to be obtained easily, is good in reaction selectivity, is less in by-products and is high in yield. The employed raw materials are all low-toxic or toxic-free and are all corrosiveness-free so that the method is not rigorous in requirement of devices, is environmental-friendly and is suitable for industrialized production.

Preparation of alkenyl-lactic acid esters and the novel esters obtained

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, (2008/06/13)

A process for the preparation of an alkenyl-lactic acid ester by reaction of a cyanohydrin with an alcohol in the presence of hydrogen chloride, followed by hydrolysis. The compounds obtained may be used for the preparation of alkaloids and crop protection agents, and as monomers for copolymerization.

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