532223
5-Amino-1,3-dimethylpyrazole
97%
Autenticatiper visualizzare i prezzi riservati alla tua organizzazione & contrattuali
Scegli un formato
Cambia visualizzazione
10 G
CHF 169.00
About This Item
Formula empirica (notazione di Hill):
C5H9N3
Numero CAS:
Peso molecolare:
111.15
Numero MDL:
Codice UNSPSC:
12352100
ID PubChem:
NACRES:
NA.22
Saggio
97%
Punto di fusione
65-69 °C (lit.)
Stringa SMILE
Cc1cc(N)n(C)n1
InChI
1S/C5H9N3/c1-4-3-5(6)8(2)7-4/h3H,6H2,1-2H3
ZFDGMMZLXSFNFU-UHFFFAOYSA-N
Categorie correlate
Descrizione generale
5-Amino-1,3-dimethylpyrazole undergoes cyclocondensation with ethyl acetoacetate to form the corresponding tetrahydropyrazolopyridine derivatives.
Applicazioni
5-Amino-1,3-dimethylpyrazole may be used in the preparation of:
- 5-benzamido-1,3-dimethylpyrazole[1]
- diethyl 2-{[(1,3-dimethyl-1H-pyrazol-5-yl)amino]methylene}malonate[2]
- 5-amino-1,3-dimethyl-4-phthalidylpyrazole
- (E)-N-(3,7-dimethylocta-2,6-dienyl)-1,3-dimethyl-1H-pyrazol-5-amine analog(LQFM002)[3]
- 4-isopropyl-1,3-dimethyl-1H-pyrazolo[3,4-b]pyridin-6-ol
Avvertenze
Warning
Indicazioni di pericolo
Consigli di prudenza
Classi di pericolo
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Organi bersaglio
Respiratory system
Codice della classe di stoccaggio
11 - Combustible Solids
Classe di pericolosità dell'acqua (WGK)
WGK 3
Punto d’infiammabilità (°F)
190.4 °F - closed cup
Punto d’infiammabilità (°C)
88 °C - closed cup
Dispositivi di protezione individuale
dust mask type N95 (US), Eyeshields, Gloves
Scegli una delle versioni più recenti:
Possiedi già questo prodotto?
I documenti relativi ai prodotti acquistati recentemente sono disponibili nell’Archivio dei documenti.
The reaction of o?phthalaldchydic acid with 5?amino?1,3?dimethylpyrazole.
Swett LR and Aynilian GH.
Journal of Heterocyclic Chemistry, 12(6), 1135-1136 (1975)
1,3-Oxazines and related compounds. II.1) Ring contraction reaction of 1, 3-oxazin-4-one derivatives into 1,2,4-triazoles and pyrazoles.
Yamamoto, et al.
Chemical & Pharmaceutical Bulletin, 26(6), 1825-1831 (1978)
E A Costa et al.
Life sciences, 92(3), 237-244 (2013-01-09)
The current study describes the synthesis and pharmacological evaluation of (E)-N-(3,7-dimethylocta-2,6-dienyl)-1,3-dimethyl-1H-pyrazol-5-amine (LQFM002), a compound originally designed through a molecular simplification strategy from 4-nerolidylcatechol. LQFM002 was evaluated for preservation of the PLA(2) enzyme inhibitory effects of the lead compound, 4-nerolidylcatechol, using
The cyclocondensation of 5?amino?1,3?dimethylpyrazole with ethyl acetoacetate. Synthesis of isomeric pyrazolopyridones.
Ratajczyk JD and Swett LR.
Journal of Heterocyclic Chemistry, 12(3), 517-522 (1975)
Hiroshi Ochiai et al.
Chemical & pharmaceutical bulletin, 52(9), 1098-1104 (2004-09-02)
A series of 4-anilinopyrazolopyridine derivatives were synthesized and biologically evaluated as inhibitors of phosphodiesterase (PDE4). Chemical modification of 3, a structurally new chemical lead that was found in our in-house library, was focused on 1- and 3-substituents. Full details of
Active Filters
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.
