CAS 3446-89-7

4-(Metiltio)benzaldeide

Descrizione:

4-(Metiltio)benzaldeide, con il numero CAS 3446-89-7, è un composto organico caratterizzato da un gruppo funzionale benzaldeidico sostituito da un gruppo metiltio nella posizione para. Questo composto appare generalmente come un liquido incolore o giallo pallido con un odore aromatico distintivo. È solubile in solventi organici come etanolo ed etere, ma ha una solubilità limitata in acqua a causa del suo gruppo metiltio idrofobico. La presenza del gruppo metiltio conferisce una reattività unica, rendendolo utile in varie applicazioni sintetiche, inclusa la produzione di farmaci e agrochimici. Inoltre, 4-(Metiltio)benzaldeide può partecipare a reazioni di addizione nucleofila e può fungere da blocco di costruzione nella sintesi organica. I dati di sicurezza indicano che deve essere maneggiato con cura, poiché può causare irritazione alla pelle, agli occhi e al sistema respiratorio. Si raccomandano adeguate precauzioni di sicurezza, incluso l'uso di dispositivi di protezione individuale, quando si lavora con questo composto.

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

Sinonimi:

• 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, 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

Purezza: 97%

Colore e forma: Clear colorless to pale yellow, Liquid

Peso molecolare: 152.21

Ref: 02-B25427

Benzaldehyde, 4-​(methylthio)​-

CAS: 3446-89-7

Formula: C₈H₈OS

Purezza: 95%

Colore e forma: Liquid

Peso molecolare: 152.2135

Ref: IN-DA003LS6

4-(Methylthio)benzaldehyde

CAS: 3446-89-7

Formula: C₈H₈OS

Purezza: ≥ 98.0%

Colore e forma: Colourless to yellow liquid

Peso molecolare: 152.22

Ref: 7W-GK7243

4-(Methylthio)benzaldehyde

CAS: 3446-89-7

4-(Methylthio)benzaldehyde

Formula: C₈H₈OS

Purezza: 98%

Colore e forma: clear. colourless to faint yellow liquid

Peso molecolare: 152.21g/mol

Ref: 54-OR0776

4-(Methylthio)benzaldehyde

CAS: 3446-89-7

Formula: C₈H₈OS

Purezza: >97.0%(GC)

Colore e forma: White to Yellow to Green clear liquid

Peso molecolare: 152.21

Ref: 3B-M0739

4-(Methylthio)benzaldehyde

CAS: 3446-89-7

Formula: C₈H₈OS

Purezza: 95%

Colore e forma: Clear

Peso molecolare: 152.21

Ref: 10-F402351

4-(Methylthio)benzaldehyde

Prodotto controllato

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

Colore e forma: Neat

Peso molecolare: 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.

Purezza: Min. 95%

Ref: 3D-FM36588