Protein Information

Name CHCH
Synonyms CHCH; CHURC 1; CHURC1; Chch; Churchill domain containing 1; Churchill protein; My015; Chches…

Compound Information

Name OCH
CAS 2,3,4,4,5,5,6,6-octachloro-2-cyclohexen-1-one

Reference List

PubMed Abstract RScore(About this table)
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 butanone 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) methane ligands. Inorg Chem. 2009 Feb 2;48(3):936-45.


The third-generation bis (1-pyrazolyl) methane 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 hydrogen bond. J Phys Chem A. 2006 Aug 24;110(33):10163-8.


The estimated interaction energies of the benzene 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