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检测方案
99%
形式
solid
bp
82 °C/60 mmHg (lit.)
mp
31-33 °C (lit.)
SMILES字符串
Oc1ccc(OC(F)(F)F)cc1C=O
InChI
1S/C8H5F3O3/c9-8(10,11)14-6-1-2-7(13)5(3-6)4-12/h1-4,13H
InChI key
WQUZBERVMUEJTD-UHFFFAOYSA-N
一般描述
2-Hydroxy-5-(trifluoromethoxy)benzaldehyde is formed as intermediate during the biotransformation pathways of CP-122,721 in humans.
应用
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
警示用语：
Warning
危险声明
危险分类
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
WGK
WGK 3
闪点(°F)
closed cup
闪点(°C)
closed cup
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
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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