CAS 16982-21-1

Ethyl thiooxamate

Description:

Ethyl thiooxamate is an organic compound characterized by its thioamide functional group, which features a sulfur atom bonded to a carbon atom that is also connected to an ethyl group and an oxime moiety. This compound typically appears as a colorless to pale yellow liquid or solid, depending on its purity and temperature. Ethyl thiooxamate is known for its role in organic synthesis and as a reagent in various chemical reactions, particularly in the formation of thioamides and other sulfur-containing compounds. It exhibits moderate solubility in organic solvents, making it useful in various applications within organic chemistry. The compound may also demonstrate biological activity, which has led to interest in its potential applications in pharmaceuticals and agrochemicals. However, like many thioamides, it may pose certain health and environmental risks, necessitating careful handling and adherence to safety protocols during its use. Overall, ethyl thiooxamate is a versatile compound with significant relevance in both synthetic and applied chemistry.

Formula: C₄H₇NO₂S

InChI: InChI=1/C4H7NO2S/c1-2-8-4(7)3(5)6/h2H2,1H3,(H2,5,6)

InChI key: InChIKey=YMBMCMOZIGSBOA-UHFFFAOYSA-N

SMILES: C(OCC)(C(N)=S)=O

Synonyms:

• (Amino)(thioxo)acetic acid ethyl ester
• 2-Amino-2-thioxoacetic acid ethyl ester
• 2-Thiooxamic acid ethyl ester
• Acetic acid, 2-amino-2-thioxo-, ethyl ester
• Acetic acid, aminothioxo-, ethyl ester
• Aminothioxoacetic Acid Ethyl Ester
• Ethyl 2-Amino-2-Thioxoacetate
• Ethyl 2-amino-thioxoacetate
• Ethyl 2-thiooxamate
• Ethyl Aminothioxoacetate
• Ethyl Thiooxamidate
• Ethyl Thioxamate
• Ethyl amino(thiocarbonyl)carboxylate
• Ethyl thiocarbamoylformate
• NSC 174676
• Oxamic acid, 2-thio-, ethyl ester
• S-ethyl amino(oxo)ethanethioate
• Thiooxamic Acid Ethyl Ester
• ETHYL THIOOXAMATE
• Ethyl thiooxamate, 98 %

Ethyl Thiooxamate

CAS: 16982-21-1

Formula: C₄H₇NO₂S

Purity: >98.0%(GC)(N)

Color and Shape: Light yellow to Yellow to Orange powder to crystal

Molecular weight: 133.17

Ref: 3B-E0735

Ethyl thiooxamate, 95%

CAS: 16982-21-1

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Sci

Formula: C₄H₇NO₂S

Purity: 95%

Color and Shape: Crystals or powder or crystalline powder, Yellow

Molecular weight: 133.17

Ref: 02-H31447

Ethyl thiooxamate

CAS: 16982-21-1

Ethyl thiooxamate

Formula: C₄H₇NO₂S

Purity: 97%

Color and Shape: Light red. Solid-Powder

Molecular weight: 133.16888

Ref: 54-OR10873

2-Thiooxamic acid ethyl ester

CAS: 16982-21-1

Ethyl 2-amino-2-thioxoacetate

Formula: C₄H₇NO₂S

Purity: 98%

Molecular weight: 133.17

Ref: IN-DG129531

Ethyl Thiooxamate

Controlled Product

CAS: 16982-21-1

Applications Ethyl Thiooxamate (cas# 16982-21-1) is a compound useful in organic synthesis.

Formula: C₄H₇NO₂S

Color and Shape: Neat

Molecular weight: 133.17

Ref: TR-E926850

Ethyl thiooxamate

CAS: 16982-21-1

Formula: C₄H₇NO₂S

Purity: 97%

Color and Shape: Solid

Molecular weight: 133.17

Ref: 10-F078641

Ethyl thiooxamate

CAS: 16982-21-1

Ethyl thiooxamate is a synthetic drug that binds to the allosteric binding site of protein kinases, thereby inhibiting their activity. Ethyl thiooxamate has been shown to be a potent antagonist against h9c2 cells and has been shown to inhibit acetaminophen-induced hepatotoxicity in mice. It also inhibits the activity of cholesteryl ester transfer protein, which plays an important role in the formation of low-density lipoprotein (LDL) cholesterol. This drug has been shown to have a molecular weight of 197g/mol, with an n-oxide group and two amine groups. It is synthesized by reacting tetroxide with acetamide in the presence of an asymmetric synthesis catalyst.

Formula: C₄H₇NO₂S

Purity: Min. 95%

Color and Shape: Yellow Powder

Molecular weight: 133.17 g/mol

Ref: 3D-FE07910