455-19-6 | 4-(Trifluoromethyl)benzaldehyde

Packsize	Purity	Availability	Price	Discounted Price
5g	98%	in stock	$8.00	$5.00
10g	98%	in stock	$9.00	$6.00
25g	98%	in stock	$14.00	$10.00
100g	98%	in stock	$41.00	$29.00
500g	98%	in stock	$65.00	$45.00

Description

• Catalog Number: AB66101
• Chemical Name: 4-(Trifluoromethyl)benzaldehyde
• CAS Number: 455-19-6
• Molecular Formula: C8H5F3O
• Molecular Weight: 174.1199
• MDL Number: MFCD00006952
• SMILES: O=Cc1ccc(cc1)C(F)(F)F

Computed Properties

• Complexity: 156
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 12
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 1
• XLogP3: 2.6

Literature

• Morphing the torsional potential energy function from local to global symmetry through a π link: the rotational spectrum of α,α,α-trifluoro-p-tolualdehyde.

  Chemistry (Weinheim an der Bergstrasse, Germany) 20120227

• (E)-2-[4-(Trifluoro-meth-yl)benzyl-idene]-2,3-dihydro-1H-inden-1-one.

  Acta crystallographica. Section E, Structure reports online 20120201

• Synthesis of new praziquantel analogues: potential candidates for the treatment of schistosomiasis.

  Bioorganic & medicinal chemistry letters 20120115

• Three-component reaction discovery enabled by mass spectrometry of self-assembled monolayers.

  Nature chemistry 20120101

• Ethyl 6-methyl-2-sulfanyl-idene-4-[4-(trifluoro-meth-yl)phen-yl]-1,2,3,4-tetra-hydro-pyrimidine-5-carboxyl-ate.

  Acta crystallographica. Section E, Structure reports online 20110701

• N-silyl oxyketene imines are underused yet highly versatile reagents for catalytic asymmetric synthesis.

  Nature chemistry 20101101

• On the mechanism of asymmetric allylation of aldehydes with allyltrichlorosilanes catalyzed by QUINOX, a chiral isoquinoline N-oxide.

  Journal of the American Chemical Society 20080416

• Low pressure plasma treatment of poly(3-hydroxybutyrate): toward tailored polymer surfaces for tissue engineering scaffolds.

  Journal of biomedical materials research 20020315

• Synthesis and antimycobacterial activity of new S-alkylisothiosemicarbazone derivatives.

  Bioorganic & medicinal chemistry 20020301