CAS 6332-83-8

N-[(4-chloro-3-nitrophenyl)carbamothioyl]furan-2-carboxamide

Description:

N-[(4-chloro-3-nitrophenyl)carbamothioyl]furan-2-carboxamide, with the CAS number 6332-83-8, is a chemical compound characterized by its complex structure, which includes a furan ring, a carboxamide group, and a thioamide linkage. This compound features a 4-chloro-3-nitrophenyl moiety, contributing to its potential biological activity and reactivity. The presence of the nitro group suggests possible electrophilic behavior, while the thioamide functionality may impart unique chemical properties, such as enhanced nucleophilicity. The furan ring adds to the compound's aromatic character and may influence its solubility and stability. Typically, compounds of this nature are studied for their potential applications in pharmaceuticals, agrochemicals, or as intermediates in organic synthesis. The specific interactions and reactivity of this compound can vary based on environmental conditions, such as pH and solvent polarity. Overall, N-[(4-chloro-3-nitrophenyl)carbamothioyl]furan-2-carboxamide represents a class of compounds with diverse applications in chemical research and development.

Formula: C₁₂H₈ClN₃O₄S

InChI: InChI=1/C12H8ClN3O4S/c13-8-4-3-7(6-9(8)16(18)19)14-12(21)15-11(17)10-2-1-5-20-10/h1-6H,(H2,14,15,17,21)

SMILES: c1cc(C(=NC(=Nc2ccc(c(c2)N(=O)=O)Cl)S)O)oc1

Synonyms:

• 2-Furancarboxamide, N-[[(4-chloro-3-nitrophenyl)amino]thioxomethyl]-
• N-[(4-Chloro-3-nitrophenyl)carbamothioyl]-2-furamide

2-(4-Chlorophenyl)-1-phenylethanone

CAS: 6332-83-8

Formula: C₁₄H₁₁ClO

Purity: 97%

Color and Shape: Solid

Molecular weight: 230.6895

Ref: IN-DA00EEJU

2-(4-Chlorophenyl)-1-phenylethanone

CAS: 6332-83-8

2-(4-Chlorophenyl)-1-phenylethanone

Purity: 97%

Ref: 54-OR1038674

2-(4-Chlorophenyl)acetophenone

CAS: 6332-83-8

Formula: C₁₄H₁₁ClO

Purity: 97%

Molecular weight: 230.69

Ref: 10-F022880

2-(4-Chlorophenyl)-1-phenylethanone

Controlled Product

CAS: 6332-83-8

Applications 2-(4-Chlorophenyl)-1-phenylethanone is an intermediate in the synthesis of pyrrobutamine which is antihistaminic. Also used as a reagent on the synthesis of 2,3-diaryl-6,7-dihydro-5H-1,4-diazepines which display antileukemic annd antiplatelet properties.
References Casy, A.F., et al.: J. Pharm. Pharmacol., 22, 270 (1970); Ramajayam, R., et al.: Eur, J. Med. Chem., 43, 2004 (2008);

Formula: C₁₄H₁₁ClO

Color and Shape: Neat

Molecular weight: 230.69

Ref: TR-C377865

2-(4-Chlorophenyl)acetophenone

CAS: 6332-83-8

2-(4-Chlorophenyl)acetophenone is a synthetic compound that has been used in the synthesis of other compounds. It has been shown to have affinity for chloride ions and can be used as a substitute for hydrochloric acid. 2-(4-Chlorophenyl)acetophenone has been shown to react with sodium hydroxide in a stepwise manner, forming sodium chloride as an intermediate product. This reaction is believed to be due to the high nucleophilicity of chlorine ions. The molecular descriptors of this compound include four bonds, one ring, two heteroatoms, and two double bonds. This chemical also displays functional theory characteristics such as elimination and leishmania inhibition.

Formula: C₁₄H₁₁ClO

Purity: Min. 95%

Molecular weight: 230.69 g/mol

Ref: 3D-GAA33283