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3-METHYL-2-BUTEN-1-YL THIOLACETATE is an organic compound that serves as a precursor to 3-Methyl-2-butenyl-1-thiol, a molecule that is highly susceptible to oxidation to form the disulfide. 3-METHYL-2-BUTEN-1-YL THIOLACETATE is known for its reactivity and instability, making it a valuable intermediate in various chemical synthesis processes.

33049-93-3

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33049-93-3 Usage

Uses

Used in Chemical Synthesis:
3-METHYL-2-BUTEN-1-YL THIOLACETATE is used as a precursor for the synthesis of 3-Methyl-2-butenyl-1-thiol, which is an unstable compound. It plays a crucial role in the preparation of various chemical compounds and materials due to its reactivity and ability to undergo oxidation.
Used in Research and Development:
In the field of research and development, 3-METHYL-2-BUTEN-1-YL THIOLACETATE is utilized for the study of its properties and potential applications. Scientists and researchers can request a detailed procedure for the preparation of the thiol from the thioacetate, along with spectral data, to further explore its characteristics and possible uses.
Used in Pharmaceutical and Agrochemical Industries:
3-METHYL-2-BUTEN-1-YL THIOLACETATE may also find applications in the pharmaceutical and agrochemical industries as an intermediate for the synthesis of various active ingredients and compounds. Its reactivity and ability to form disulfide bonds can be leveraged in the development of new drugs and agrochemical products.

Check Digit Verification of cas no

The CAS Registry Mumber 33049-93-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,0,4 and 9 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 33049-93:
(7*3)+(6*3)+(5*0)+(4*4)+(3*9)+(2*9)+(1*3)=103
103 % 10 = 3
So 33049-93-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H12OS/c1-6(2)4-5-9-7(3)8/h4H,5H2,1-3H3

33049-93-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name S-(3-methylbut-2-enyl) ethanethioate

1.2 Other means of identification

Product number -
Other names 3-Methyl-2-butenyl acetothioate

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:33049-93-3 SDS

33049-93-3Relevant academic research and scientific papers

Liquid sulfur as a reagent: Synthesis of polysulfanes with 20 or more sulfur atoms with characterization by UPLC-(Ag+)-coordination ion spray-MS

Wang, Kai,Groom, Murree,Sheridan, Robert,Zhang, Shaozhong,Block, Eric

, p. 55 - 66 (2013/08/24)

Diallyl disulfide reacts within minutes with liquid sulfur at 120°C giving a family of diallyl polysulfanes, All2S n (n=3-22), characterized by ultra-performance liquid chromatography-(Ag+)-coordination ion spray-mass spectrometry (UPLC-(Ag+)CIS-MS). Similarly, garlic oil (GO), bis-(2-methyl-2-propenyl), bis-(2-chloro-2-propenyl), bis-(3-methyl-2- butenyl), and bis-(2-cyclohexen-1-yl) disulfides all give families of polysulfanes with up to 22 sequential sulfur atoms. New members of families of silver chelators with up to 10 sulfur atoms were found in GO using UPLC-(Ag +)CIS-MS. 2013 Copyright Taylor and Francis Group, LLC.

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