D182001
3,5-Dimethylpyrazole
99%
Synonym(s):
3,5-Dimethyl-1H-pyrazole
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About This Item
Empirical Formula (Hill Notation):
C5H8N2
CAS Number:
Molecular Weight:
96.13
NACRES:
NA.22
PubChem Substance ID:
eCl@ss:
39160503
UNSPSC Code:
12352100
EC Number:
200-657-5
MDL number:
Beilstein/REAXYS Number:
106325
Assay:
99%
Form:
powder
InChI key
SDXAWLJRERMRKF-UHFFFAOYSA-N
InChI
1S/C5H8N2/c1-4-3-5(2)7-6-4/h3H,1-2H3,(H,6,7)
SMILES string
Cc1cc(C)[nH]n1
assay
99%
form
powder
bp
218 °C (lit.)
Quality Level
mp
105-108 °C (lit.)
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Related Categories
Application
Common reagent for the preparation of pyrazolato ligated complexes. Also used to prepare N-1-substituted derivatives having antibacterial activity.
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - STOT RE 2
target_organs
Liver
Storage Class
13 - Non Combustible Solids
wgk
WGK 3
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Journal of Organometallic Chemistry, 443, 221-221 (1993)
J. Chem. Soc., Dalton Trans., 3625-3625 (1993)
J. Chem. Soc. Pak., 14, 125-125 (1992)
Rupam Sarma et al.
Dalton transactions (Cambridge, England : 2003), (36)(36), 7428-7436 (2009-09-04)
The reactions of 3,5-dimethylpyrazole with zinc(II)acetate dihydrate and varieties of aromatic carboxylic acids led to formation of mono-nuclear zinc complexes of composition [Zn(HDMP)2(RCO2)2] (R = C6H5, p-CH3-C6H4, p-NO2-C6H4 etc. HDMP = 3,5-dimethylpyrazole) in methanol, whereas the same reactants in dimethylformamide
A Del Roso et al.
Acta biologica Hungarica, 42(1-3), 87-99 (1991-01-01)
In this study, we explored the changes in the rate of protein degradation in liver cells in vivo, using a method based on the physiological stimulation of liver autophagy. Male albino rats 1, 2, 6, 12 and 24 months old
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