CAS 3446-89-7

4-(Methylthio)benzaldehyde

Description:

4-(Methylthio)benzaldehyde, with the CAS number 3446-89-7, is an organic compound characterized by a benzaldehyde functional group substituted with a methylthio group at the para position. This compound typically appears as a colorless to pale yellow liquid with a distinctive aromatic odor. It is soluble in organic solvents such as ethanol and ether but has limited solubility in water due to its hydrophobic methylthio group. The presence of the methylthio group imparts unique reactivity, making it useful in various synthetic applications, including the production of pharmaceuticals and agrochemicals. Additionally, 4-(Methylthio)benzaldehyde can participate in nucleophilic addition reactions and can serve as a building block in organic synthesis. Safety data indicates that it should be handled with care, as it may cause irritation to the skin, eyes, and respiratory system. Proper safety precautions, including the use of personal protective equipment, are recommended when working with this compound.

Formula: C₈H₈OS

InChI: InChI=1S/C8H8OS/c1-10-8-4-2-7(6-9)3-5-8/h2-6H,1H3

InChI key: InChIKey=QRVYABWJVXXOTN-UHFFFAOYSA-N

SMILES: C(=O)C1=CC=C(SC)C=C1

Synonyms:

• 4-(Methylmercapto)benzaldehyde
• 4-(Methylsulfanyl)Benzaldehyde
• 4-(Methylthio)benzaldehyde
• 4-Formylthioanisole
• 4-Methanesulfanylbenzaldehyde
• 4-Methanethiobenzaldehyde
• 4-Methyl-Thio Benzaldehyde
• 4-Methylbenzenecarbothialdehyde
• 4-Methylsulfanylbenzaldehyde
• Benzaldehyde, 4-(methylthio)-
• Benzaldehyde, p-(methylthio)-
• Methyl 4-formylphenyl thioether

4-(Methylthio)benzaldehyde

CAS: 3446-89-7

Formula: C₈H₈OS

Purity: >97.0%(GC)

Color and Shape: White to Yellow to Green clear liquid

Molecular weight: 152.21

Ref: 3B-M0739

4-(Methylthio)benzaldehyde, 97%

CAS: 3446-89-7

4-(Methylthio)benzaldehyde is a building block for the synthesis of various pharmaceutical and biologically active compounds. It can be used for the synthesis of sulfur-containing terpyridine ligands. It is the intermediate for the synthesis of a class of pyrrole derivatives showing analgesic/anti-i

Formula: C₈H₈OS

Purity: 97%

Color and Shape: Clear colorless to pale yellow, Liquid

Molecular weight: 152.21

Ref: 02-B25427

Benzaldehyde, 4-​(methylthio)​-

CAS: 3446-89-7

Formula: C₈H₈OS

Purity: 95%

Color and Shape: Liquid

Molecular weight: 152.2135

Ref: IN-DA003LS6

4-(Methylthio)benzaldehyde

CAS: 3446-89-7

4-(Methylthio)benzaldehyde

Formula: C₈H₈OS

Purity: 98%

Color and Shape: clear. colourless to faint yellow liquid

Molecular weight: 152.21g/mol

Ref: 54-OR0776

4-(Methylthio)benzaldehyde

CAS: 3446-89-7

Formula: C₈H₈OS

Purity: ≥ 98.0%

Color and Shape: Colourless to yellow liquid

Molecular weight: 152.22

Ref: 7W-GK7243

4-(Methylthio)benzaldehyde

CAS: 3446-89-7

Formula: C₈H₈OS

Purity: 95%

Color and Shape: Clear

Molecular weight: 152.21

Ref: 10-F402351

4-(Methylthio)benzaldehyde

CAS: 3446-89-7

Formula: C₈H₈OS

Ref: TR-TRC-M330660

4-(Methylthio)benzaldehyde

Controlled Product

CAS: 3446-89-7

Applications 4-(Methylthio)benzaldehyde, is a building block for the synthesis of various pharmaceutical and biologically active compounds. It can be used for the synthesis of sulfur-containing terpyridine ligands. It is the intermediate for the synthesis of a class of pyrrole derivatives showing analgesic/anti-inflammatory activity.
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package
References Romashkina, R. B., et al.: Russian Chemical Bulletin, 61, 2265 (2012); Battilocchio, C., et al.: Bioorg. Med. Chem., 21, 3695 (2013);

Formula: C₈H₈OS

Color and Shape: Neat

Molecular weight: 152.21

Ref: TR-M330660

4-Methylthio benzaldehyde

CAS: 3446-89-7

4-Methylthio benzaldehyde is an organic compound that has been used in the synthesis of benzalkonium chloride, a bacteriostatic agent. This chemical has been studied for its toxicological properties and is not considered to be a carcinogen or mutagen. 4-Methylthio benzaldehyde is used in vitro to study the skin's reaction to irritants and enhancers. It has also shown genotoxic effects in vitro at high concentrations. The reaction between 4-methylthio benzaldehyde and sodium hydroxide solution produces hydrogen bonds that are important for understanding the mechanism of this chemical's activity.

Purity: Min. 95%

Ref: 3D-FM36588