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经验公式(希尔记法):
C9H8N2
化学文摘社编号:
分子量:
144.17
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
237-246-5
MDL number:
Assay:
98%
产品名称
5-甲基喹喔啉, 98%
InChI key
CQLOYHZZZCWHSG-UHFFFAOYSA-N
InChI
1S/C9H8N2/c1-7-3-2-4-8-9(7)11-6-5-10-8/h2-6H,1H3
SMILES string
Cc1cccc2nccnc12
assay
98%
refractive index
n20/D 1.62 (lit.)
bp
120 °C/15 mmHg (lit.)
mp
20-21 °C (lit.)
density
1.125 g/mL at 25 °C
Quality Level
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Application
5-Methylquinoxaline was used in the synthesis of 1,12-diphenyl-5-methyl-1,12,12a,12b-tetrahydrobis[1,2,4]triazolo[4,3-a:3′,4′-c]quinoxaline bis-cycloadducts.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
10 - Combustible liquids
wgk
WGK 3
flash_point_f
235.4 °F - closed cup
flash_point_c
113 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
Reactivity of asymmetric benzo-condensed diazines with nitrilimine dipoles in the 1, 3-dipolar cycloaddition reactions.
Tetrahedron Letters, 50(52), 7333-7336 (2009)
Ecem Berk et al.
Journal of agricultural and food chemistry, 67(17), 4923-4930 (2019-04-11)
This study investigated the formation of Maillard reaction products in sesame seeds under different roasting conditions. Sesame seeds were roasted at 150, 180, 200, and 220 °C for 10 min, and thermal process contaminants including 5-hydroxymethylfurfural, acrylamide, furan, and dicarbonyl
Weerachat Sompong et al.
BMC complementary and alternative medicine, 15, 394-394 (2015-11-02)
Methylglyoxal (MG) is one of the most reactive glycating agents, which result the formation of advanced glycation end-products (AGEs) that have been implicated in the progression of age-related diseases. Inhibition of MG-induced AGE formation is the imperative approach for alleviating
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