Name | CHCH |
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Synonyms | CHCH; CHURC 1; CHURC1; Chch; Churchill domain containing 1; Churchill protein; My015; Chches… |
Name | OCH |
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CAS | 2,3,4,4,5,5,6,6-octachloro-2-cyclohexen-1-one |
PubMed | Abstract | RScore(About this table) | |
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19044817 | Fitzpatrick BL, Lau KC, Butler LJ, Lee SH, Lin JJ: Investigation of the O+allyl addition/elimination reaction pathways from the OCH (2) CHCH (2) radical intermediate. J Chem Phys. 2008 Aug 28;129(8):084301. |
4(0,0,0,4) | Details |
11666239 | Lindner E, Schreiber R, Schneller T, Wegner P, Mayer HA, Gopel W, Ziegler C: Synthesis of Polysiloxane-Bound (Ether-phosphine) palladium Complexes. Inorg Chem. 1996 Jan 17;35(2):514-525. The reaction of two equiv of the monomeric ether-phosphine O,P ligand (MeO)(3) Si (CH (2))(3)(Ph) PCH (2)-Do [1a (T (0)()), 1b (T (0)())] {Do = CH (2) OCH (3) [1a (T (0)())], CHCH (2) CH (2) CH (2) O [1b (T (0)())]} with PdCl (2)(COD) yields the monomeric palladium (II) complexes Cl (2) Pd (P approximately O)(2) [2a (T (0)())(2)(), 2b (T (0)())(2)()]. |
2(0,0,0,2) | Details |
19228051 | Kaiser EW, Wallington TJ, Hurley MD: Products and mechanism of the reaction of Cl with in N2/O2 diluent at 297-526 K. J Phys Chem A. 2009 Mar 19;113(11):2424-37. Rate constant ratios of k (CH (2) C (O) C (2) H (5) + Cl (2))/k (CH (2) C (O) C (2) H (5) + O (2)) = 0.027 +/- 0.008, k (CH (3) C (O) CHCH (3) + Cl (2))/ k (CH (3) C (O) CHCH (3) + O (2)) = 0.0113 +/- 0.0011, and k (CH (3) C (O) CH (2) CH (2) + Cl (2))/k (CH (3) C (O) CH (2) CH (2) + O (2)) = 1.52 +/- 0.32 were determined at 297 K in 800-950 Torr of N (2) diluent. |
1(0,0,0,1) | Details |
19119870 | Reger DL, Foley EA, Smith MD: Mononuclear metallacyclic silver (I) complexes of third generation bis (1-pyrazolyl) ligands. Inorg Chem. 2009 Feb 2;48(3):936-45. The third-generation bis (1-pyrazolyl) ligands p-C (6) H (4)[CH (2) OCH (2) CH (pz)(2)](2) (L (p), pz = pyrazolyl ring) and m-C (6) H (4)[CH (2) OCH (2) CH (pz)(2)](2) (L (m)) have been synthesized by the reaction of (pz)(2) CHCH (2) OH with NaH followed by alpha,alpha'-dibromo-p-xylene or alpha,alpha'-dibromo-m-xylene. |
1(0,0,0,1) | Details |
16913692 | Tsuzuki S, Honda K, Uchimaru T, Mikami M, Fujii A: Magnitude and directionality of the interaction energy of the aliphatic CH/pi interaction: significant difference from bond. J Phys Chem A. 2006 Aug 24;110(33):10163-8. The estimated interaction energies of the complexes with CH (4), CH (3) CH (3), CH (2) CH (2), CHCH, CH (3) NH (2), CH (3) OH, CH (3) OCH (3), CH (3) F, CH (3) Cl, CH (3) ClNH (2), CH (3) ClOH, CH (2) Cl (2), CH (2) FCl, CH (2) F (2), CHCl (3), and CH (3) F (3) are -1.45, -1.82, -2.06, -2.83, -1.94, -1.98, -2.06, -2.31, -2.99, -3.57, -3.71, -4.54, -3.88, -3.22, -5.64, and -4.18 kcal/mol, respectively. |
1(0,0,0,1) | Details |
18970885 | Chandra S, Buschbeck R, Lang H: A 15-crown-5-functionalized carbosilane dendrimer as ionophore for ammonium selective electrodes. Talanta. 2006 Dec 15;70(5):1087-93. Epub 2006 Mar 27. The synthesis of CH (2) CHCH (2) OCH (2)[15-crown-5] (III) is achieved by the treatment of HOCH (2)- [15-crown-5] (I) with equimolar amounts of CH (2) CHCH (2) Br (II) in the presence of KOH. |
1(0,0,0,1) | Details |