SCHEMBL556803

SCHEMBL556803

C=C[Si](C)(C)OC(C)C

nearest known ligand 0.00

⚠ Novel chemotype — no close known analogue (best Tanimoto < 0.3). Unexplored chemical space relative to ChEMBL.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
SCHEMBL8759231 0.86
SCHEMBL31343129 0.82
SCHEMBL27772225 0.80
SCHEMBL3622090 0.77
SCHEMBL537977 0.77
SCHEMBL5823076 0.74
SCHEMBL17874989 0.74
SCHEMBL4265425 0.74
SCHEMBL17598568 0.73
SCHEMBL3627762 0.73

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Claimed or disclosed in 81 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-9074032-B2 Membranes based on polyvinyl alcohol WACKER CHEMIE AG (DE) 2015-07-07 US claimed
EP-2414411-B1 MEMBRANES BASED ON POLYVINYL ALCOHOL WACKER CHEMIE AG (DE) 2013-02-20 EP claimed
CN-102875810-A Phenyl-containing MT type resin and preparation method thereof ZHONGHAO CHENGUANG RES INST CHEMICAL INDUSTRY 2013-01-16 CN claimed
US-20120031843-A1 Membranes based on polyvinyl alcohol WACKER CHEMIE AG (DE) 2012-02-09 US claimed
US-20110021460-A1 SELECTIVE HYDROSILYLATION METHOD AND PRODUCT MOMENTIVE PERFORMANCE MATERIALS, INC. 2011-01-27 US claimed
US-7834118-B2 Selective hydrosilylation method with rhodium catalyst MOMENTIVE PERFORMANCE MATERIALS INC (US) 2010-11-16 US claimed
US-20080081924-A1 SELECTIVE MOLAR EXCESS HYDROSILYLATION METHOD AND PRODUCT MOMENTIVE PERFORMANCE MATERIALS INC. 2008-04-03 US claimed
US-20080076896-A1 SELECTIVE HYDROSILYLATION METHOD AND PRODUCT MOMENTIVE PERFORMANCE MATERIALS INC. 2008-03-27 US claimed
US-20080076939-A1 Two-step process of reacting a dihydroorganosiloxane with a terminally unsaturated compound in the presence of a rhodium catalyst and then with a different unsaturated compound to form an assymetrically disubstitued siloxane; one of the unsaturated compounds is an alkenyl polyalkylene oxide MOMENTIVE PERFORMANCE MATERIALS INC. 2008-03-27 US claimed
US-7326761-B1 Selective hydrosilylation method and product GENERAL ELECTRIC COMPANY (US) 2008-02-05 US claimed
US-20080015325-A1 SELECTIVE HYDROSILYLATION METHOD AND PRODUCT MOMENTIVE PERFORMANCE MATERIALS INC. 2008-01-17 US claimed
US-20080015323-A1 SELECTIVE HYDROSILYLATION METHOD AND PRODUCT MOMENTIVE PERFORMANCE MATERIALS INC. 2008-01-17 US claimed
US-20080015324-A1 Use of tris(dibutylsulfide)rhodium trichloride catalyst to make a siloxane-functional polyoxyalkylene glycol; use as a hydrolysis resistant-imparting agent for a composition in need of hydrolysis resistance such as agrochemical, personal care, and home care formulations MOMENTIVE PERFORMANCE MATERIALS INC. 2008-01-17 US claimed
US-7259220-B1 Selective hydrosilylation method GENERAL ELECTRIC COMPANY (US) 2007-08-21 US claimed
US-20240122814-A1 DENTAL ADHESIVE COMPOSITION TOKUYAMA DENTAL CORPORATION (JP) 2024-04-18 US disclosed
EP-4327798-A1 DENTAL ADHESIVE COMPOSITION Tokuyama Dental Corporation (JP) 2024-02-28 EP disclosed
WO-2022224807-A1 DENTAL ADHESIVE COMPOSITION 株式会社トクヤマデンタル 2022-10-27 WO disclosed
WO-1998026028-A1 FUEL COMPOSITIONS EXHIBITING IMPROVED FUEL STABILITY ORR WILLIAM C (US) 1998-06-18 WO disclosed
US-4883344-A MULTILAYER FERROELECTRIC ELEMENT/STABILITY CANON KABUSHIKI KAISHA (JP) 1989-11-28 US disclosed
US-4820026-A UNIFORMITY, STABILITY, LARGE TILT ANGLE; INCLUDING UNSATURATED SILICON MONOMER CANON KABUSHIKI KAISHA (JP) 1989-04-11 US disclosed