342157
2-羟基-5-(三氟甲氧基)苯甲醛
99%
别名:
5-(三氟甲氧基)水杨醛
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关于此项目
线性分子式:
CF3OC6H3(OH)CHO
化学文摘社编号:
分子量:
206.12
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
99%
Form:
solid
InChI
1S/C8H5F3O3/c9-8(10,11)14-6-1-2-7(13)5(3-6)4-12/h1-4,13H
SMILES string
Oc1ccc(OC(F)(F)F)cc1C=O
InChI key
WQUZBERVMUEJTD-UHFFFAOYSA-N
assay
99%
form
solid
bp
82 °C/60 mmHg (lit.)
mp
31-33 °C (lit.)
Application
2-Hydroxy-5-(trifluoromethoxy)benzaldehyde may be used in the preparation of :
- 2-[(E)-2-hydroxy-5-(trifluoromethoxy)benzylideneamino]-4-methylphenol
- (E)-2-((3-fluorophenylimino)methyl)-4-(trifluoromethoxy) phenol
- 2-[(E)-(naphthalen-2-ylimino) methyl]-4-(trifluoromethoxy) phenol
General description
2-Hydroxy-5-(trifluoromethoxy)benzaldehyde is formed as intermediate during the biotransformation pathways of CP-122,721 in humans.
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
235.4 °F - closed cup
flash_point_c
113 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
此项目有
Aslı Tosyalı Karadağ et al.
Acta crystallographica. Section E, Structure reports online, 67(Pt 1), o95-o95 (2010-01-01)
The title compound, C(15)H(12)F(3)NO(3), is a Schiff base which adopts the cis-quinoid form in the solid state. The dihedral angle between the least-squares planes of the benzene rings being 3.6 (1)°. The F atoms of the -CF(3) group are disordered over
Yelda Bingöl Alpaslan et al.
Acta crystallographica. Section E, Structure reports online, 66(Pt 3), o510-o510 (2010-01-01)
The title compound, C(14)H(9)F(4)NO(2), is a Schiff base which adopts the phenol-imine tautomeric form in the solid state. The H atom is located on the hydr-oxy O atom rather than on the N atom. This H atom is involved in
2-[(E)-(Naphthalen-2-ylimino) methyl]-4-(trifluoromethoxy) phenol.
Pekdemir M, et al.
Acta Crystallographica Section E, Structure Reports Online, 68(4), o10204-o10204 (2012)
Kevin Colizza et al.
Drug metabolism and disposition: the biological fate of chemicals, 35(6), 884-897 (2007-03-16)
The metabolism, pharmacokinetics, and excretion of a potent and selective substance P receptor antagonist, CP-122,721 [(+)-(2S,3S)-3-(2-methoxy-5-trifluoromethoxybenzylamino)-2-phenylpiperidine], have been studied in six healthy male human subjects [four extensive metabolizers (EMs) and two poor metabolizers (PMs) of CYP2D6) following oral administration of
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