추천 제품
Quality Level
분석
99%
양식
powder
bp
218 °C (lit.)
mp
105-108 °C (lit.)
SMILES string
Cc1cc(C)[nH]n1
InChI
1S/C5H8N2/c1-4-3-5(2)7-6-4/h3H,1-2H3,(H,6,7)
InChI key
SDXAWLJRERMRKF-UHFFFAOYSA-N
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애플리케이션
Common reagent for the preparation of pyrazolato ligated complexes. Also used to prepare N-1-substituted derivatives having antibacterial activity.
신호어
Warning
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 4 Oral - STOT RE 2
표적 기관
Liver
Storage Class Code
13 - Non Combustible Solids
WGK
WGK 3
개인 보호 장비
dust mask type N95 (US), Eyeshields, Gloves
이미 열람한 고객
J. Chem. Soc., Dalton Trans., 3625-3625 (1993)
J. Chem. Soc. Pak., 14, 125-125 (1992)
Journal of Organometallic Chemistry, 443, 221-221 (1993)
P Masiello et al.
Metabolism: clinical and experimental, 51(1), 110-114 (2002-01-10)
This study intended to test the hypothesis that intracellular lipolysis in the pancreatic beta cells is implicated in the regulation of insulin secretion stimulated by nutrient secretagogues or cyclic adenosine monophosphate (cAMP) agonists. Indeed, although lipid signaling molecules were repeatedly
V Krishnakumar et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 79(5), 1959-1968 (2011-06-28)
In this work, the experimental and theoretical vibrational spectra of pyrazole (PZ) and 3,5-dimethyl pyrazole (DMP) have been studied. FTIR and FT-Raman spectra of the title compounds in the solid phase are recorded in the region 4000-400 cm(-1) and 4000-50
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