Passa al contenuto
Merck
Tutte le immagini(2)

Documenti fondamentali

Visualizza tutta la documentazione

128376

Sigma-Aldrich

4-Fluorobenzaldehyde

98%

Sinonimo/i:

p-Fluorobenzaldehyde

Autenticatiper visualizzare i prezzi riservati alla tua organizzazione & contrattuali
Tutte le immagini(2)

About This Item

Formula condensata:
FC6H4CHO
Numero CAS:
459-57-4
Peso molecolare:
124.11
Beilstein:
385857
Numero CE:
207-293-6
Numero MDL:
MFCD00003378
Codice UNSPSC:
12352100
ID PubChem:
24847852
NACRES:
NA.22

Livello qualitativo

100

Saggio

98%

Stato

liquid

Indice di rifrazione

n20/D 1.521 (lit.)

P. ebollizione

181 °C/758 mmHg (lit.)

Punto di fusione

−10 °C (lit.)

Densità

1.157 g/mL at 25 °C (lit.)

Gruppo funzionale

aldehyde
fluoro

Stringa SMILE

[H]C(=O)c1ccc(F)cc1

InChI

1S/C7H5FO/c8-7-3-1-6(5-9)2-4-7/h1-5H
UOQXIWFBQSVDPP-UHFFFAOYSA-N

Cerchi prodotti simili? Visita Guida al confronto tra prodotti

Categorie correlate

Descrizione generale

4-Fluorobenzaldehyde, also known as p-Fluorobenzaldehyde is an organic compound often used in the condensation reactions for the synthesis of phenolic monomers.

Applicazioni

4-Fluorobenzaldehyde was used in the preparation of pyrazolopyridine UR-13756.

Avvertenze

Warning

Indicazioni di pericolo

H226,H302,H319,H411

Classi di pericolo

Acute Tox. 4 Oral - Aquatic Chronic 2 - Eye Irrit. 2 - Flam. Liq. 3

Codice della classe di stoccaggio

3 - Flammable liquids

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

132.8 °F - closed cup

Punto d’infiammabilità (°C)

56 °C - closed cup

Dispositivi di protezione individuale

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

Scegli una delle versioni più recenti:

Certificati d'analisi (COA)

Lot/Batch Number
MKCP8592
MKCL4601
MKCK5020
MKCK5022
MKCK5023

Non trovi la versione di tuo interesse?

Se hai bisogno di una versione specifica, puoi cercare il certificato tramite il numero di lotto.

Cerca un COA

Possiedi già questo prodotto?

I documenti relativi ai prodotti acquistati recentemente sono disponibili nell’Archivio dei documenti.

Visita l’Archivio dei documenti

I clienti hanno visto anche

Slide 1 of 6

1 of 6

4-Iodobenzaldehyde 96%

Sigma-Aldrich

263826

4-Iodobenzaldehyde

2,4,6-Tri-(4-fluorophenyl)pyrylium tetrafluoroborate ≥95%

Sigma-Aldrich

902136

2,4,6-Tri-(4-fluorophenyl)pyrylium tetrafluoroborate

4-Nitrobenzaldehyde 98% (GC)

Sigma-Aldrich

130176

4-Nitrobenzaldehyde

3,4-Difluorobenzaldehyde 97%

Sigma-Aldrich

265160

3,4-Difluorobenzaldehyde

p-Anisaldehyde 98%

Sigma-Aldrich

A88107

p-Anisaldehyde

4-Cyanobenzaldehyde for synthesis

Sigma-Aldrich

8.18530

4-Cyanobenzaldehyde

Abdul Hafeez et al.
Polymers, 11(9) (2019-09-22)
Bis-aldehyde monomers 4-(4'-formyl-phenoxy)benzaldehyde (3a), 3-methoxy-4-(4'-formyl-phenoxy)benzaldehyde (3b), and 3-ethoxy-4-(4'-formyl-phenoxy)benzaldehyde (3c) were synthesized by etherification of 4-fluorobenzaldehyde (1) with 4-hydroxybenzaldehyde (2a), 3-methoxy-4-hydroxybenzaldehyde (2b), and 3-ethoxy-4-hydroxybenzaldehyde (2c), respectively. Each monomer was polymerized with p-phenylenediamine and 4,4'-diaminodiphenyl ether to yield six poly(azomethine)s. Single crystal
Mark C Bagley et al.
Future medicinal chemistry, 2(2), 193-201 (2011-03-24)
UR-13756 is a potent and selective p38 mitogen-activated protein kinase (MAPK) inhibitor, reported to have good bioavailability and pharmacokinetic properties and, thus, is of potential use in the treatment of accelerated aging in Werner syndrome. Irradiation of 2-chloroacrylonitrile and methylhydrazine
Xuemei Tian et al.
Enzyme and microbial technology, 84, 32-40 (2016-02-02)
The first Novozym 435 lipase-catalyzed Morita-Baylis-Hillman (MBH) reaction with amides as co-catalyst was realized. Results showed that neither Novozym 435 nor amide can independently catalyze the reaction. This co-catalytic system that used a catalytic amount of Novozym 435 with a
Ana Margarida Araújo et al.
Archives of toxicology, 92(11), 3307-3323 (2018-09-27)
3,4-Methylenedioxymethamphetamine (MDMA, ecstasy) is a well-known hepatotoxic drug. Although its toxicity has been thoroughly studied at high concentrations, there is still insufficient knowledge on possible alterations of cell function at subtoxic concentrations, which are in fact more representative concentrations of
Bin-Yu Wen et al.
Journal of Asian natural products research, 21(7), 702-715 (2019-01-01)
Desmosdumotin C (Des C), a natural product isolated from the roots of Desmos dumosus, has shown good antitumor activity. A three dimensional quantitative structure-activity relationship (QSAR) study using the comparative molecular field analysis (CoMFA) method was performed on 32 Des
Visualizza tutti i documenti correlati

Global Trade Item Number

SKUGTIN
128376-10G4061838725523
128376-25G
128376-500G
128376-100G
128376-250G4061838725530
128376-50G4061838725547

Il team dei nostri ricercatori vanta grande esperienza in tutte le aree della ricerca quali Life Science, scienza dei materiali, sintesi chimica, cromatografia, discipline analitiche, ecc..

Contatta l'Assistenza Tecnica.