[PH2B-[CH2PPH2-(2)]]-PD-[N,C:ETA2-N-CY2CHCH3]
Compound with spectra: 2 NMR
![[PH2B-[CH2PPH2-(2)]]-PD-[N,C:ETA2-N-CY2CHCH3]](/api/compound/KZulEJTyEZH.png?ph=true&h=300&w=458 "[PH2B-[CH2PPH2-(2)]]-PD-[N,C:ETA2-N-CY2CHCH3]")
| SpectraBase Compound ID | KZulEJTyEZH |
|---|---|
| InChI | InChI=1S/C38H34BP2.C14H26N.Pd/c1-7-19-33(20-8-1)39(34-21-9-2-10-22-34,31-40(35-23-11-3-12-24-35)36-25-13-4-14-26-36)32-41(37-27-15-5-16-28-37)38-29-17-6-18-30-38;1-2-15(13-9-5-3-6-10-13)14-11-7-4-8-12-14;/h1-30H,31-32H2;2,13-14H,3-12H2,1H3;/q-1;;-1/p+2 |
| InChIKey | FNXZFWVIGADKMR-UHFFFAOYSA-P |
| Mol Weight | 880.3 g/mol |
| Molecular Formula | C52H62BNP2Pd |
| Exact Mass | 879.348535 g/mol |
| Parent InChIKey | LSKDEPQCXBVELH-UHFFFAOYSA-P |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
[PH2B-[CH2PPH2-(2)]]-PD-[N,C:ETA2-N-IPR2CHCH2CH3]
2-(4-Methylphenylamino)-1-[(o-(triphenylphosphanyl)imino)phenyl]indazolo[3,2-e][1,2,4]triazole
2-(4-Methoxyphenylamino)-1-[(o-(triphenylphosphanyl)imino)phenyl]indazolo[3,2-e][1,2,4]triazole
5,5'-bis(Benzyloxy)-7,7',9,9'-tetramethoxy-1,1',3,3'-tetramethyl-1H,1'H-8,8'-dibenzo[g]isochromene
1-Benzothiophene-3-carboxylic acid, 4,5,6,7-tetrahydro-2-[[2-(1-methyl-2-phenyl-1H-indol-3-yl)-1,2-dioxoethyl]amino]-, ethyl ester
1-ALPHA-ACETOXY-5-BETA-HYDROXYEUDESM-4(15)-EN-6-BETA,11-BETA-H-12,6-OLIDE
10-Cyclohexyl-2,3,3a,4,5,6-hexahydro-4-(2-oxetanyl)-1H-pyrazino[3,2,1-j,k]carbazole
ACETYL-ARTEMIN
2-Amino-4-(4-methoxyphenyl)-5,8-dioxo-8,9-dihydro-5H-pyrido[3,2-e]thiazolo[3,2-a]pyrimidine-3-carbonitrile
12-[1',2'-Dihydroxyethyl)-modified HEME
| Title | Journal or Book | Year |
|---|---|---|
| Synthetic, Structural, and Mechanistic Aspects of an Amine Activation Process Mediated at a Zwitterionic Pd(II) Center | Journal of the American Chemical Society | 2004 |