165190
邻乙酰水杨酰氯
95%
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线性分子式:
2-(CH3CO2)C6H4COCl
化学文摘社编号:
分子量:
198.60
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
226-899-1
Beilstein/REAXYS Number:
880372
MDL number:
产品名称
邻乙酰水杨酰氯, 95%
InChI key
DSGKWFGEUBCEIE-UHFFFAOYSA-N
InChI
1S/C9H7ClO3/c1-6(11)13-8-5-3-2-4-7(8)9(10)12/h2-5H,1H3
SMILES string
CC(=O)Oc1ccccc1C(Cl)=O
assay
95%
form
solid
refractive index
n20/D 1.536 (lit.)
bp
107-110 °C/0.1 mmHg (lit.)
mp
45-49 °C (lit.)
functional group
acyl chloride
ester
Quality Level
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Application
- O-Acetylsalicyloyl chloride was used in the synthesis of enantiomerically pure bidentate heteroorganic ligands built on simple achiral skeletons and containing an aziridine moiety.
- It was used in the general synthesis of acetoxybenzamides.
- It was used in the chemical synthesis of 2,2,6,6-tetramethyl-1-piperidinyloxy(TEMPO)-aspirin conjugate via condensation reaction with 4-hydroxy-TEMPO.
- It was used as reagent in acylation of cyclobutenediones.
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1B
存储类别
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
230.0 °F
flash_point_c
110 °C
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
法规信息
新产品
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Wilmarie Flores-Santana et al.
British journal of pharmacology, 165(4b), 1058-1067 (2011-06-11)
Inflammation and reactive oxygen species are associated with the promotion of various cancers. The use of non-steroidal anti-inflammatory drugs (NSAIDs) in cancer prevention treatments has been promising in numerous cancers. We report the evaluation of NSAIDs chemically modified by the
The Journal of Organic Chemistry, 58, 3543-3543 (1993)
Aziridine ring-containing chiral ligands as highly efficient catalysts in asymmetric synthesis.
Rachwalski M, et al.
Tetrahedron Asymmetry, 24(7), 421-425 (2013)
Carlos Barea et al.
Bioorganic & medicinal chemistry letters, 21(15), 4498-4502 (2011-07-05)
Continuing with our efforts to identify new active compounds against malaria and leishmaniasis, 14 new 3-amino-1,4-di-N-oxide quinoxaline-2-carbonitrile derivatives were synthesized and evaluated for their in vitro antimalarial and antileishmanial activity against Plasmodium falciparum Colombian FCR-3 strain and Leishmania amazonensis strain
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