1,4-Dimethylbenzene CAS 68650-36-2 WIKI information includes physical and chemical properties, USES, security data, NMR spectroscopy, computational chemical data and more.
Provied information about 2-Chloro-1,4-dimethylbenzene(Molecular Formula: C8H9Cl, CAS Registry Number:95-72-7 ) ,Boiling Point,Melting Point,Flash Point,Density, NMR Molecular Structure,Risk Codes,Synthesis Route at guidechem
CAS号:15540-84-8 CAS号15540-84-8, 分子量为263.95, 分子式C8H8Br2, 标准纯度98%, 毕得医药(Bidepharm)提供15540-84-8批次质检(如NMR, HPLC, GC)等检测报告。(请以英文为准,中文仅做参考) 2,3-Dibromo-1,4-dimethylbenzene 货号:BD01809442 2,3-Dibromo-1,4-dimethylbenzene , 98% ...
别名对二甲苯-d10 | 1,4-二甲苯-d10 英文别名D99434 | MFCD00037699 | A935671 | URLKBWYHVLBVBO-ZGYYUIRESA-N | [2H10]-1,4-Dimethylbenzene | p-Xylene-d10, 99 atom % D | 1,4-Dimethylbenzene-d10 | (2H10)-p-Xylene | DTXSID70194021 | 2-Xylene-d10; para-Xylene-d10; 1,4-Dimeth...
p-Xylene-d10, 99+ atom % D, for NMR 1,4-dimethylbenzene-d10 1,4-Dimethylbenzene-D10 99.5 Atom % D p-Xylene-d10, 99%(Isotopic) 1,4-Bis(2H3)methyl(2,3,5,6-2H4)benzene 1,4-Bis[(2H3)methyl](2,3,5,6-2H4)benzene
Compound OMEGA,OMEGA'-BIS-(1,5-BIS-(2-METHYLPROPYL)-2,4-DIOXOHEXAHYDRO-1,3,5-TRIAZINYL)-1,4-DIMETHYLBENZENEwith free spectra: 1 NMR.
1-BROMO-3,4-DIMETHYLBENZENE 3,4-DIMETHYLBROMOBENZENE 4-BROMO-1,2-DIMETHYLBENZENE 4-Bromo-1,2-xylene 4-BROMO-O-XYLENE 5-BROMO-O-XYLENE ρ-Bromo-o-xylene 3,4-dimethylphenylbromide 3,4-Xylyl bromide 3,4-xylylbromide 4-bromo-1,2-dimethyl-benzen ...
3,5-二甲基-1,2-苯二胺; 3,5-二甲基-1,2-亚苯基二胺; (2-氨基-4,6-二甲基-苯基)胺; 3,5-二甲基苯-1,2-二胺; 英文同义名: 3,5-Dimethyl-1,2-phenylenediamine; 3,5-DIMETHYLBENZENE-1,2-DIAMINE; m-Xylene-4,5-diamine; (2-amino-3,5-dimethylphenyl)amine(SALTDATA: FREE); 1,2-Di...
ChemInform Abstract: INVESTIGATION OF METHYL REORIENTATIONS IN 1,4‐DIMETHOXY‐2,6‐DIMETHYLBENZENE BY NMR AND INELASTIC NEUTRON SCATTERINGstructure (organic substances)No abstract is available for this article.doi:10.1002/chin.197932099R. A. WIND...
Step 1. Synthesis of N1-(2-chloro-6-phenyl-pyrimidin-4-yl)-N3,N3-dimethyl-benzene-1,3-diamine (Intermediate B.3)Titled compound was obtained using intermediate A (300 mg, 1.13 mmol) and N1,N1-dimethylbenzene-1,3-diamine (181.5 mg, 1.33 mmol) following the general procedure reaction B ...