Welcome to LookChem.com Sign In|Join Free
  • or
[(Methoxythioxomethyl)thio]acetic acid, also known as methoxythioxomethylthioacetic acid, is a chemical compound with the formula C4H6O3S2. It is a thiolactic acid derivative characterized by its thioxomethyl and thioacetic acid functional groups, which provide potential applications in organic synthesis and as a building block for constructing more complex molecules.

16323-12-9

Post Buying Request

16323-12-9 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

16323-12-9 Usage

Uses

Used in Pharmaceutical Industry:
[(Methoxythioxomethyl)thio]acetic acid is used as an intermediate in the synthesis of various drugs. Its unique functional groups allow for the creation of a wide range of pharmaceutical compounds, contributing to the development of new medications.
Used in Agricultural Industry:
In the agricultural industry, [(methoxythioxomethyl)thio]acetic acid is utilized as an intermediate in the production of crop protection products. Its versatility in chemical reactions enables the synthesis of various agrochemicals that help protect crops from pests and diseases.
Used in Organic Synthesis:
[(Methoxythioxomethyl)thio]acetic acid is used as a building block for constructing more complex molecules in organic synthesis. Its thioxomethyl and thioacetic acid functional groups make it a valuable component in the creation of intricate chemical structures.
Used in Pharmaceutical Research and Development:
[(Methoxythioxomethyl)thio]acetic acid is used as a versatile reagent for the preparation of various thioesters and thioacetic acid derivatives. These compounds are essential in the research and development of new pharmaceuticals, driving innovation in the field of medicine.

Check Digit Verification of cas no

The CAS Registry Mumber 16323-12-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,3,2 and 3 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 16323-12:
(7*1)+(6*6)+(5*3)+(4*2)+(3*3)+(2*1)+(1*2)=79
79 % 10 = 9
So 16323-12-9 is a valid CAS Registry Number.
InChI:InChI=1/C4H6O3S2/c1-7-4(8)9-2-3(5)6/h2H2,1H3,(H,5,6)

16323-12-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(methoxycarbonothioylthio)acetic acid

1.2 Other means of identification

Product number -
Other names [(Methoxythioxomethyl)thio]acetic acid

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:16323-12-9 SDS

16323-12-9Relevant academic research and scientific papers

Bifunctional 2-(alkoxycarbonothioylthio)acetic acids for the synthesis of TiO2-poly(vinyl acetate) nanocomposites via RAFT polymerization

Xiao, Shude,Xu, William Z.,Charpentier, Paul A.

, p. 606 - 618 (2014/02/14)

Reversible addition-fragmentation chain-transfer (RAFT) polymerization has been known as a convenient method for the synthesis of polymers of designed molecular structures. Of particular interest are bifunctional or multifunctional chain-transfer agents (CTAs) which could be employed in the development of advanced materials via RAFT polymerization. In the present study, four bifunctional 2-(alkoxycarbonothioylthio) RAFT CTAs with i£ COOH functionalities containing methoxy, ethoxy, isopropoxy, and octyloxy groups, respectively, were synthesized and characterized by FTIR and NMR spectroscopy. Polymerizations of vinyl acetate using these CTAs exhibited increased molecular weight with consumption of monomer and relatively narrow dispersities, indicative of living polymerization behavior. The effect of the concentration of 2-(ethoxycarbonothioylthio) acetic acid on the polymerization was examined, revealing that higher concentration of CTA led to lower molecular weight and narrower dispersity. As an example of the application of the synthesized bifunctional CTAs, TiO2-poly(vinyl acetate) (PVAc) nanocomposites were synthesized via a one-pot process and characterized by TGA, DSC, TEM, and affinity test, suggesting attachment of PVAc onto the nano-TiO2 particles. Copyright

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 16323-12-9