Results 11 to 20 of about 46,343 (254)

4-(Benzyloxy)benzaldehyde [PDF]

open access: yesActa Crystallographica Section E Structure Reports Online, 2010
The title compound, C(14)H(12)O(2), has an essentially planar conformation with the two aromatic rings forming a dihedral angle of 5.23 (9)° and the aldehyde group lying in the plane of its aromatic group [maximum deviation = 0.204 (3) Å]. Weak inter-molecular C-H⋯O contacts are found to be shortest between the aldehyde O-atom acceptor and the H atoms ...
Kennedy, Alan R.   +3 more
openaire   +5 more sources

Benzaldehyde thiosemicarbazone monohydrate [PDF]

open access: yesActa Crystallographica Section E Structure Reports Online, 2008
In the title compound, C(8)H(9)N(3)S·H(2)O, intra-molecular N-H⋯N hydrogen bonding contributes to the mol-ecular conformation. Water mol-ecules are involved in inter-molecular N-H⋯O and O-H⋯S hydrogen bonds, which link the mol-ecules into ribbons extended along the a axis.
Sheng-Jiu Gu, Kai-Mei Zhu
openaire   +3 more sources

Mechanisms of Antimicrobial Action of Cinnamon and Oregano Oils, Cinnamaldehyde, Carvacrol, 2,5-Dihydroxybenzaldehyde, and 2-Hydroxy-5-Methoxybenzaldehyde against Mycobacterium avium subsp. paratuberculosis (Map)

open access: yesFoods, 2017
The antimicrobial modes of action of six naturally occurring compounds, cinnamon oil, cinnamaldehyde, oregano oil, carvacrol, 2,5-dihydroxybenzaldehyde, and 2-hydroxy-5-methoxybenzaldehyde, previously found to inhibit the growth of Mycobacterium avium ...
Stella W. Nowotarska   +5 more
doaj   +1 more source

Scientific Opinion on Flavouring Group Evaluation 20, Revision 3(FGE.20Rev3): Benzyl alcohols, benzaldehydes, a related acetal, benzoic acids, and related esters from chemical groups 23 and 30

open access: yesEFSA Journal, 2011
The Panel on Food Contact Materials, Enzymes, Flavourings and Processing Aids of the European Food Safety Authority was requested to consider in this revision 3 of Flavouring Group Evaluation 20, the SCF Opinion on benzoic acid.
EFSA Panel on Food Contact Materials, Enzymes, Flavourings and Processing Aids (CEF)
doaj   +1 more source

Organocatalytic atroposelective heterocycloaddition to access axially chiral 2-arylquinolines

open access: yesCommunications Chemistry, 2021
2-Arylquinoline derivatives are key components of many enantioselective catalysts, but existing synthetic routes are few in number. Here atroposelective aminocatalytic aza-Michael addition of amino-benzaldehydes to iminium intermediates yields single ...
Gongming Yang   +4 more
doaj   +1 more source

2-(Phenylmethylthio)benzaldehyde [PDF]

open access: yesActa Crystallographica Section C Crystal Structure Communications, 1995
In the title compound, C 14 H 12 OS, the two planar benzaldehyde and benzyl groups are inclined at 77.7(1)°. The torsion angle about the central C-S bond is 174.9 (2)°. The molecules are held together in the crystal by van der Waals interactions.
Lee, SM, Wong, WT
openaire   +3 more sources

Titania-Catalyzed H2O2 Thermal Oxidation of Styrenes to Aldehydes

open access: yesMolecules, 2019
We investigated the selective oxidation of styrenes to benzaldehydes by using a non-irradiated TiO2−H2O2 catalytic system. The oxidation promotes multi-step reactions from styrenes, including the cleavage of a C=C double bond and the addition of an
Satoru Ito   +6 more
doaj   +1 more source

Chemo-Selective Protection of Aldehydes Functional Group Catalyzed by MOFs

open access: yesChemistry Proceedings, 2022
A metal-organic framework Zn2(BDC)2(DABCO) was employed as a reusable heterogeneous acidic catalyst in the acylation reaction of various benzaldehydes with acetic anhydride under microwave irradiation.
Sakineh Mahdian   +2 more
doaj   +1 more source

4-(Methylsulfonyl)benzaldehyde [PDF]

open access: yesActa Crystallographica Section E Structure Reports Online, 2009
In the crystal of the title compound, C(8)H(8)O(3)S, the mol-ecules are linked into a three-dimensional array by inter-molecular C-H⋯O hydrogen bonds.
Hong-You Cui, Shao-Song Qian
openaire   +3 more sources

Antifungal activity of redox-active benzaldehydes that target cellular antioxidation

open access: yesAnnals of Clinical Microbiology and Antimicrobials, 2011
Background Disruption of cellular antioxidation systems should be an effective method for control of fungal pathogens. Such disruption can be achieved with redox-active compounds.
Mahoney Noreen   +3 more
doaj   +1 more source

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