⚠ 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.
| Compound | similarity | top predicted | shared targets | |
|---|---|---|---|---|
| SCHEMBL9771423 | 0.91 | — | — | |
| SCHEMBL27388505 | 0.74 | — | — | |
| SCHEMBL16027140 | 0.70 | — | — | |
| SCHEMBL875275 | 0.70 | — | — | |
| 1,1-Dichloroethene SCHEMBL28185378 | 0.67 | — | — | |
| Ethylene SCHEMBL26121191 | 0.60 | — | — | |
| SCHEMBL368827 | 0.59 | — | — | |
| SCHEMBL1020286 | 0.59 | — | — | |
| SCHEMBL30922366 | 0.58 | — | — | |
| Hypochlorous Acid SCHEMBL482943 | 0.58 | — | — |
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 139 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-5977419-A | Process for the preparation of substituted phenylpropenes | BAYER AKTIENGESELLSCHAFT (DE) | 1999-11-02 | — | — | US | claimed |
| EP-0436989-B1 | Process for rearranging allylic geminal dihalogen compounds | DOWELANCO (US) | 1995-03-22 | — | — | EP | claimed |
| US-5072063-A | Catalytic isomerization of 3,3-dihalopropene; continuous processing of by-product stream components; high yield and selectivity; chemical intermediates | DOWELANCO (US) | 1991-12-10 | — | — | US | claimed |
| EP-0436989-A1 | Process for rearranging allylic geminal dihalogen compounds | DOWELANCO (US) | 1991-07-17 | — | — | EP | claimed |
| US-4492800-A | Process for the preparation of 1,1-dichloro-alkenes | BAYER AKTIENGESELLSCHAFT (DE) | 1985-01-08 | — | — | US | claimed |
| US-4460793-A | REACTING 1,1-DICHLOROALKENE AND PHENOLATE TO OBTAIN PHENYLETHER INTERMEDIATE, ACID HYDROLYSIS | BAYER AKTIENGESELLSCHAFT (DE) | 1984-07-17 | — | — | US | claimed |
| EP-0055427-B1 | PROCESS FOR THE PRODUCTION OF MONOCHLOROMETHYL KETONES | BAYER AG (DE) | 1984-05-02 | — | — | EP | claimed |
| EP-0035754-B1 | PROCESS FOR MANUFACTURING 1,1-DICHLORO-ALKENES | BAYER AG (DE) | 1983-08-24 | — | — | EP | claimed |
| EP-0035753-B1 | PROCESS FOR MANUFACTURING 1,1-DICHLORO-ALKENES | BAYER AG (DE) | 1983-06-22 | — | — | EP | claimed |
| US-4350824-A | Process for the preparation of 1,1-dichloro-alkenes | BAYER AKTIENGESELLSCHAFT (DE) | 1982-09-21 | — | — | US | claimed |
| US-4342704-A | BY REACTION OF AN ALDEHYDE WITH A DICHLOROMETHANE PHOSPHONIC ACID ESTER | BAYER AKTIENGESELLSCHAFT (DE) | 1982-08-03 | — | — | US | claimed |
| US-3951614-A | REACTION PRODUCT OF A HYDROCARBYL AMINE AND POLYFUNCTIONAL COUPLING AGENT | CHEVRON RESEARCH COMPANY (US) | 1976-04-20 | — | — | US | claimed |
| JP-1254634-A | — | — | None | — | — | JP | disclosed |
| JP-6340561-A | — | — | None | — | — | JP | disclosed |
| CN-122055058-A | Biaryl compound and method for controlling plant disease | 住友化学株式会社 | 2026-05-15 | — | — | CN | disclosed |
| CN-122029166-A | Condensed cyclic compound and harmful arthropod control composition containing the same | 住友化学株式会社 | 2026-05-12 | — | — | CN | disclosed |
| EP-0023598-A1 | Process for the preparation of 1,1-dichloro alkenes | BAYER AG (DE) | 1981-02-11 | — | — | EP | disclosed |
| EP-0022984-A1 | Process for the preparation of derivatives of 3-(2.2-dichloro-vinyl)-2.2-dimethyl-cyclopropane-1-carboxylic acid | BAYER AG (DE) | 1981-01-28 | — | — | EP | disclosed |
| EP-0022971-A1 | Process for the preparation of 3-(2,2-dichlorovinyl)-2,2-dimethyl-cyclopropane-1-carboxylic acid derivatives | BAYER AG (DE) | 1981-01-28 | — | — | EP | disclosed |
| US-3951614-A | REACTION PRODUCT OF A HYDROCARBYL AMINE AND POLYFUNCTIONAL COUPLING AGENT | CHEVRON RESEARCH COMPANY (US) | 1976-04-20 | — | — | US | disclosed |