CAS 4521-33-9

5-Nitro-2-thiophenecarboxaldehyde

Description:

5-Nitro-2-thiophenecarboxaldehyde is an organic compound characterized by the presence of a thiophene ring, a nitro group, and an aldehyde functional group. Its molecular structure features a five-membered aromatic ring containing sulfur, which contributes to its unique chemical properties. The nitro group (-NO2) is an electron-withdrawing substituent that can influence the reactivity of the compound, making it useful in various synthetic applications. The aldehyde group (-CHO) is reactive and can participate in condensation reactions, making this compound valuable in organic synthesis. 5-Nitro-2-thiophenecarboxaldehyde is typically a yellow to brown solid and is soluble in organic solvents. It is often used in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals due to its ability to undergo further chemical transformations. Safety precautions should be taken when handling this compound, as nitro compounds can be hazardous. Overall, its unique structure and functional groups make it an interesting subject of study in organic chemistry.

Formula: C₅H₃NO₃S

InChI: InChI=1S/C5H3NO3S/c7-3-4-1-2-5(10-4)6(8)9/h1-3H

InChI key: InChIKey=CHTSWZNXEKOLPM-UHFFFAOYSA-N

SMILES: N(=O)(=O)C=1SC(C=O)=CC1

Synonyms:

• 2-Formyl-5-nitrothiophene
• 2-Nitrothiophene-5-carboxaldehyde
• 2-Thiophenecarboxaldehyde, 5-nitro-
• 5-Nitro-2-formylthiophene
• 5-Nitro-2-thienaldehyde
• 5-Nitro-2-thienylaldehyde
• 5-Nitro-2-thienylcarboxaldehyde
• 5-Nitro-2-thiophenealdehyde
• 5-Nitro-2-thiophenecarboxaldehyde
• 5-Nitrothiophene-2-carbaldehyde
• NSC 168226
• 5-NITROTHIOPHENE-2-CARBOXALDEHYDE
• 5-Nitrothiophene-2-carboxaldehyde,98%
• AKOS 93853
• LABOTEST-BB LT00112375
• 5-NITRO-2-THIOPHENECARBALDEHYDE

5-Nitrothiophene-2-carboxaldehyde, 98%

CAS: 4521-33-9

5-Nitrothiophene-2-carboxaldehyde is used as a chemical for protoemics research as well as the synthesis of 2,3-dihydro-2-(5-nitro-2-thienyl) quinazolin-4-(1H)-ones1 and various novel oxime ether derivatives which are anti-protozoan agents. This Thermo Scientific Chemicals brand product was original

Formula: C₅H₃NO₃S

Purity: 98%

Color and Shape: Cream to yellow to green to brown to gray, Crystals or powder or crystalline powder or lumps or fused solid or needles

Molecular weight: 157.14

Ref: 02-L01493

5-Nitrothiophene-2-carboxaldehyde

CAS: 4521-33-9

Formula: C₅H₃NO₃S

Purity: 98%

Color and Shape: Solid

Molecular weight: 157.1472

Ref: IN-DA003MXJ

5-Nitrothiophene-2-Carboxaldehyde

CAS: 4521-33-9

5-Nitrothiophene-2-Carboxaldehyde

Purity: 98%

Molecular weight: 157.15g/mol

Ref: 54-OR1011921

5-Nitrothiophene-2-carboxaldehyde

CAS: 4521-33-9

Formula: C₅H₃NO₃S

Purity: 90%

Color and Shape: Solid

Molecular weight: 157.14

Ref: 10-F037376

5-Nitrothiophene-2-carboxaldehyde

Controlled Product

CAS: 4521-33-9

Applications 5-Nitrothiophene-2-carboxaldehyde is a reagent that is used in the activity of mefloquine-oxazolidine derivatives against multidrug-resistant Mycobacterium tuberculosis.
References Goncalves, R. S. B., et al.: Bioorg. Med. Chem., 20, 243 (2012);

Formula: C₅H₃NO₃S

Color and Shape: Neat

Molecular weight: 157.15

Ref: TR-N565510

5-Nitrothiophene-2-carboxaldehyde

CAS: 4521-33-9

5-Nitrothiophene-2-carboxaldehyde (5NT) is a chemical compound that belongs to the class of dihedral molecules. It is commonly used as an antimicrobial agent and has been shown to have amoebicidal activity in tissue culture. 5NT also inhibits cell growth and proliferation in certain bacteria, such as Staphylococcus aureus strains, by interfering with DNA replication and protein synthesis. Although 5NT is not active against other types of bacteria, it has been shown to be effective against MRSA in laboratory studies. The biological properties of 5NT are still being studied.

Formula: C₅H₃NO₃S

Purity: Min. 95%

Molecular weight: 157.15 g/mol

Ref: 3D-FN33032