C94807
3-Pyridinecarbonitrile
98%
Sinonimo/i:
3-Cyanopyridine, Nicotinic acid nitrile, Nicotinonitrile
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About This Item
Formula empirica (notazione di Hill):
C6H4N2
Numero CAS:
Peso molecolare:
104.11
Beilstein:
107711
Numero CE:
Numero MDL:
Codice UNSPSC:
12352100
ID PubChem:
NACRES:
NA.22
Prodotti consigliati
![[Pd(OAc)2]3 reagent grade, 98%](/deepweb/assets/sigmaaldrich/product/structures/508/249/99a0ef2c-b77c-4d73-8ed9-0cca05b6b41f/640/99a0ef2c-b77c-4d73-8ed9-0cca05b6b41f.png)
Livello qualitativo
Saggio
98%
Stato
crystals
Impurezze
<2.5% acetone
P. ebollizione
201 °C (lit.)
Punto di fusione
48-52 °C (lit.)
Stringa SMILE
N#Cc1cccnc1
InChI
1S/C6H4N2/c7-4-6-2-1-3-8-5-6/h1-3,5H
GZPHSAQLYPIAIN-UHFFFAOYSA-N
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Categorie correlate
Avvertenze
Danger
Indicazioni di pericolo
Consigli di prudenza
Classi di pericolo
Acute Tox. 4 Oral - Eye Dam. 1 - Skin Irrit. 2
Codice della classe di stoccaggio
11 - Combustible Solids
Classe di pericolosità dell'acqua (WGK)
WGK 3
Punto d’infiammabilità (°F)
190.4 °F
Punto d’infiammabilità (°C)
88 °C
Dispositivi di protezione individuale
dust mask type N95 (US), Eyeshields, Gloves
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I clienti hanno visto anche
Win-Long Chia et al.
International journal of molecular sciences, 14(9), 18809-18823 (2013-09-17)
A new series of teraryl 2-(4'-alkoxybiphen-4-yl)-5-cyanopyridines (nO-PPPyCN, n = 2-8) compounds, bearing a cyanopyridine terminus, were synthesized using a short 2-step reaction with overall yields between 33% and 69%. Spectral analyses were in accord with the expected structures. Thermotropic behavior
Mika Takahashi et al.
Reproductive toxicology (Elmsford, N.Y.), 35, 7-16 (2012-11-21)
Crl:CD(SD)rats were given 3-cyanopyridine by gavage at 0, 5, 30 or 180 mg/kg/day. Males were dosed for 42 days beginning 14 days before mating, and females for 40-53 days beginning 14 days before mating to day 3 of lactation, including
Xiaolin Pei et al.
Biotechnology letters, 35(9), 1419-1424 (2013-04-24)
A nitrile hydratase (NHase) gene from Aurantimonas manganoxydans, cloned and expressed in Escherichia coli, gave an enzyme that efficiently hydrated 3-cyanopyridine to nicotinamide with high thermal stability. We have now found that adding Co(2+) at 0.1 mM to LB medium was
Synthesis and antihistaminic activity of 2-guanadino-3-cyanopyridines and pyrido[2,3-d]-pyrimidines.
J M Quintela et al.
Bioorganic & medicinal chemistry, 5(8), 1543-1553 (1997-08-01)
2-Guanadino-3-cyanopyridines 8-33 and pyrido[2,3-d]-pyrimidines 35-52 were synthesized by nucleophilic displacement and cyclization of the chloroamidines 6a-d easily obtained by reaction of 2-aminocyanopyridines 5a-d with phosgene iminium chloride and their action on the release of histamine by mast cells examined under
Y Kato et al.
Archives of microbiology, 170(2), 85-90 (1998-07-31)
A bacterial strain capable of utilizing E-pyridine-3-aldoxime as a nitrogen source was isolated from soil after a 4-month acclimation period and was identified as Rhodococcus sp. The strain contained a novel aldoxime dehydration activity that catalyzed a stoichiometric dehydration of
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