T46108
1,2,4-Triazole
98%
동의어(들):
3,4-Diazapyrrole, 4H-1,2,4-Triazole, s-Triazole (8CI)
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크기 선택
보기 변경
제품정보 (DICE 배송 시 비용 별도)
실험식(Hill 표기법):
C2H3N3
CAS 번호:
Molecular Weight:
69.07
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
206-022-9
Beilstein/REAXYS Number:
104767
MDL number:
Assay:
98%
Quality Level
assay
98%
bp
260 °C (lit.)
mp
119-121 °C (lit.)
SMILES string
c1nc[nH]n1
InChI
1S/C2H3N3/c1-3-2-5-4-1/h1-2H,(H,3,4,5)
InChI key
NSPMIYGKQJPBQR-UHFFFAOYSA-N
Application
1,2,4-triazole and its derivatives are important structural moieties of many pharmaceutical drugs. Triazoles can also act as ligands to form coordination complexes with transition metal ions. Due to their electron-deficient nature, they exhibit excellent electron-transport and hole-blocking properties, making them promising organic materials in material science applications.
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signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Repr. 1B
저장 등급
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 2
flash_point_f
338.0 °F
flash_point_c
170 °C
ppe
Eyeshields, Gloves, type P3 (EN 143) respirator cartridges
Applications of Metal-Free 1, 2, 4-Triazole Derivatives in Materials Science.
Diaz-Ortiz A
Current Organic Chemistry, 19(7), 568-584 (2015)
Mononuclear, oligonuclear and polynuclear metal coordination compounds with 1, 2, 4-triazole derivatives as ligands.
Haasnoot JG
Coordination Chemistry Reviews, 200, 131-185 (2000)
1, 2, 4-Triazoles: Synthetic approaches and pharmacological importance.
Al-Masoudi IA
Chemistry of Heterocyclic Compounds, 42(11), 1377-1403 (2006)