ethyl 4-fluorocyclohex-3-ene-1-carboxylate - CAS 452333-58-3
Catalog: |
BB025796 |
Product Name: |
ethyl 4-fluorocyclohex-3-ene-1-carboxylate |
CAS: |
452333-58-3 |
Synonyms: |
4-fluoro-1-cyclohex-3-enecarboxylic acid ethyl ester; ethyl 4-fluorocyclohex-3-ene-1-carboxylate |
IUPAC Name: | ethyl 4-fluorocyclohex-3-ene-1-carboxylate |
Description: | ethyl 4-fluorocyclohex-3-ene-1-carboxylate (CAS# 452333-58-3 ) is a useful research chemical. |
Molecular Weight: | 172.199 |
Molecular Formula: | C9H13FO2 |
Canonical SMILES: | CCOC(=O)C1CCC(=CC1)F |
InChI: | InChI=1S/C9H13FO2/c1-2-12-9(11)7-3-5-8(10)6-4-7/h5,7H,2-4,6H2,1H3 |
InChI Key: | KBDWYRGBBWDLTP-UHFFFAOYSA-N |
LogP: | 0.00000 |
Publication Number | Title | Priority Date |
EP-2997012-A1 | Fluoro-perhexiline compounds and their therapeutic use | 20130515 |
US-2016102058-A1 | Fluoro-perhexiline compounds and their therapeutic use | 20130515 |
WO-2014184561-A1 | Fluoro-perhexiline compounds and their therapeutic use | 20130515 |
CA-2764241-A1 | Disubstituted-aminodifluorosulfinium salts, process for preparing same and method of use as deoxofluorination reagents | 20090619 |
CA-2764241-C | Disubstituted-aminodifluorosulfinium salts, process for preparing same and method of use as deoxofluorination reagents | 20090619 |
PMID | Publication Date | Title | Journal |
20405933 | 20100521 | Aminodifluorosulfinium salts: selective fluorination reagents with enhanced thermal stability and ease of handling | The Journal of organic chemistry |
Complexity: | 199 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 172.08995782 |
Formal Charge: | 0 |
Heavy Atom Count: | 12 |
Hydrogen Bond Acceptor Count: | 3 |
Hydrogen Bond Donor Count: | 0 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 172.08995782 |
Rotatable Bond Count: | 3 |
Topological Polar Surface Area: | 26.3 |
Undefined Atom Stereocenter Count: | 1 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 1.8 |
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Related Functional Groups
Cyclohexane
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