Dichloroprop-d7

CAS : 120-36-5

Ref. TR-D436748

Informations sur le produit

• Nom: Dichloroprop-d7
• Synonymes: 2,3,3,3-tetradeuterio-2-(2,4-dichloro-3,5,6-trideuteriophenoxy)propanoic acid, (2,4-Dichlorophenoxy)Acetic Acid, (2R)-2-(2,4-dichlorophenoxy)propanoate, (2R)-2-(2,4-dichlorophenoxy)propanoic acid, (2S)-2-(2,4-dichlorophenoxy)propanoate, (2S)-2-(2,4-dichlorophenoxy)propanoic acid, 2,4-Dcppa, 2,4-Dichlorophenoxy-alpha-Propionic acid, 2,4-Dichlorophenoxypropionic acid, 2,4-Dichlorphenoxypropionic Acid, 2,4-Dichlorprop, 2,4-Dp, 2-(2,4-Dichlorophenoxy)Propanoic Acid, 2-(2,4-Dp), Af 302, Canapur DP, Celatox DP, Cornox RK, DCP, Dichloroprop, Dichlorprop, Dichlorprop acid, Diclorprop, Dicopur DP, Diprop, Hedonal DP, Herbizid DP, Nsc 39624, Propanoic acid, 2-(2,4-dichlorophenoxy)-, Propionic acid, 2-(2,4-dichlorophenoxy)-, U 46DP Fluid, α-(2,4-Dichlorophenoxy)propionic acid

Description

Applications Dichloroprop-d7 can be obtained from Phenol-d5 (P318003) which is purified here for molecular genetics applications. It is naturally found in tea leaves and plants, and has uses in the synthesis of antioxidant compounds due to the antioxidant activity caused by the phenol moiety. This structure also allows it to be used for syntheses of anti-bacterial & anti-carcinogenic compounds. This is the labelled analog.
References Nam, S. et al.: J. Agri. Chem., 60, 9097 (2012); Xia, J. et al.: J. Agri. Chem., 57, 99 (2009); Khanal, P. et al.: Carcinogenesis, 32, 545 (2011);

• Marque: TRC

Propriétés chimiques

• Masse moléculaire: 242.107
• Formule: C₉D₇HCl₂O₃
• Couleur/Forme: Neat
• InChI: InChI=1S/C9H8Cl2O3/c1-5(9(12)13)14-8-3-2-6(10)4-7(8)11/h2-5H,1H3,(H,12,13)/i1D3,2D,3D,4D,5D
• Code InChI: InChIKey=MZHCENGPTKEIGP-AAYPNNLASA-N
• SMILES: [2H]c1c([2H])c(OC([2H])(C(=O)O)C([2H])([2H])[2H])c(Cl)c([2H])c1Cl