Wszystkie zdjęcia(3)
Key Documents
374776
4-Methoxybiphenyl
97%
Synonim(y):
4-Phenylanisole
Zaloguj sięWyświetlanie cen organizacyjnych i kontraktowych
About This Item
Wzór liniowy:
C6H5C6H4OCH3
Numer CAS:
Masa cząsteczkowa:
184.23
Numer WE:
Numer MDL:
Kod UNSPSC:
12171500
Identyfikator substancji w PubChem:
NACRES:
NA.47
Polecane produkty
![1-(4′-Methyl[1,1′-biphenyl]-4-yl)ethanone AldrichCPR](/deepweb/assets/sigmaaldrich/product/structures/224/118/064dfb31-1067-44ce-bf18-d3f762028eb6/640/064dfb31-1067-44ce-bf18-d3f762028eb6.png)
Próba
97%
Postać
powder, crystals or chunks
mp
86-90 °C (lit.)
Zastosowanie
diagnostic assay manufacturing
hematology
histology
temp. przechowywania
room temp
ciąg SMILES
COc1ccc(cc1)-c2ccccc2
InChI
1S/C13H12O/c1-14-13-9-7-12(8-10-13)11-5-3-2-4-6-11/h2-10H,1H3
Klucz InChI
RHDYQUZYHZWTCI-UHFFFAOYSA-N
Zastosowanie
4-Methoxybiphenyl has been used as a standard reagent whose fluorescence intensity is associated with the fluorescence characteristics of the products of derivatization reaction for aryl halides with phenylboronic acid (PBA).
This page may contain text that has been machine translated.
Kod klasy składowania
11 - Combustible Solids
Klasa zagrożenia wodnego (WGK)
WGK 3
Temperatura zapłonu (°F)
Not applicable
Temperatura zapłonu (°C)
Not applicable
Środki ochrony indywidualnej
Eyeshields, Gloves, type N95 (US)
Wybierz jedną z najnowszych wersji:
Masz już ten produkt?
Dokumenty związane z niedawno zakupionymi produktami zostały zamieszczone w Bibliotece dokumentów.
Klienci oglądali również te produkty
J R Fry
Xenobiotica; the fate of foreign compounds in biological systems, 17(6), 751-758 (1987-06-01)
1. The metabolism of 4-methoxybiphenyl to 4-hydroxybiphenyl and its sulphate and glucuronic acid conjugates has been studied in rat isolated hepatocytes at various concentrations of 4-methoxybiphenyl. 2. The proportions of metabolites produced remained constant at concentrations of 4-methoxybiphenyl less than
A comparison of biphenyl 4-hydroxylation and 4-methoxybiphenyl O-demethylation in rat liver microsomes.
J R Fry
Biochemical pharmacology, 30(14), 1915-1919 (1981-07-15)
P Paterson et al.
Xenobiotica; the fate of foreign compounds in biological systems, 15(6), 493-502 (1985-06-01)
The rate of production of 4-hydroxybiphenyl from 4-methoxybiphenyl in hepatocytes isolated from untreated rats was essentially identical to that from biphenyl in hepatocytes isolated from rats pretreated with beta-naphthoflavone at 40 mg/kg. Similar results were obtained using liver microsomes isolated
Influence of the sulphation inhibitor, 2,6-dichloro-4-nitrophenol, on the production and conjugation, of 4-hydroxybiphenyl generated from 4-methoxybiphenyl by rat isolated hepatocytes.
J R Fry et al.
Biochemical pharmacology, 36(18), 3090-3092 (1987-09-15)
Nasz zespół naukowców ma doświadczenie we wszystkich obszarach badań, w tym w naukach przyrodniczych, materiałoznawstwie, syntezie chemicznej, chromatografii, analityce i wielu innych dziedzinach.
Skontaktuj się z zespołem ds. pomocy technicznej