528331
N-甲基-N-(2-羟乙基)-4-氨基苯醛
96%
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关于此项目
线性分子式:
(HOCH2CH2)(CH3)NC6H4CHO
化学文摘社编号:
分子量:
179.22
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
96%
InChI
1S/C10H13NO2/c1-11(6-7-12)10-4-2-9(8-13)3-5-10/h2-5,8,12H,6-7H2,1H3
SMILES string
CN(CCO)c1ccc(C=O)cc1
InChI key
JOCUIVLSLBBESN-UHFFFAOYSA-N
assay
96%
mp
66-70 °C (lit.)
functional group
aldehyde, amine, hydroxyl
Quality Level
Application
N-Methyl-N-(2-hydroxyethyl)-4-aminobenzaldehyde may be used to synthesize:
- 2,5-bis[4-(methylaminoethanol)benzylidene]cyclopentanone
- 4′-[(2-tosyloxyethyl)(methyl)amino]-4-phenyl-3-buten-2-malonitrile, a tosylate precursor
- methanesulfonic acid 2-[(4-formyl-phenyl)-methyl-amino]-ethyl ester
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Synthesis and characterization of dendritic nonlinear optical chromophore containing phenylene attached with bulky alkyl group.
Choi JJ, et al.
Macromolecular Research, 15(1), 59-64 (2007)
18F-FBM: A new PET radiotracer for imaging ?-amyloid plaques and neurofibrillary tangles.
Wang C, et al.
Journal of Nuclear Medicine, 47(1), 217P-217P (2006)
Waqas Ahmad et al.
Chemical biology & drug design, 83(6), 670-681 (2014-01-11)
Arachidonic acid and its metabolites have generated a heightened interest due to their significant role in inflammation. Inhibiting the enzymes involved in arachidonic acid metabolism has been considered as the synergistic anti-inflammatory effect. A series of novel curcumin diarylpentanoid analogues
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