2-Bromo-2'-bromo-4'-methoxyacetophenone - CAS 1183778-97-3
Catalog: |
BB004092 |
Product Name: |
2-Bromo-2'-bromo-4'-methoxyacetophenone |
CAS: |
1183778-97-3 |
Synonyms: |
2-bromo-1-(2-bromo-4-methoxyphenyl)ethanone; 2-bromo-1-(2-bromo-4-methoxyphenyl)ethanone |
IUPAC Name: | 2-bromo-1-(2-bromo-4-methoxyphenyl)ethanone |
Description: | 2-Bromo-2'-bromo-4'-methoxyacetophenone (CAS# 1183778-97-3 ) is a useful research chemical. |
Molecular Weight: | 307.97 |
Molecular Formula: | C9H8Br2O2 |
Canonical SMILES: | COC1=CC(=C(C=C1)C(=O)CBr)Br |
InChI: | InChI=1S/C9H8Br2O2/c1-13-6-2-3-7(8(11)4-6)9(12)5-10/h2-4H,5H2,1H3 |
InChI Key: | GOOOJKFZIYIHDF-UHFFFAOYSA-N |
Publication Number | Title | Priority Date |
WO-2021150918-A1 | 4,5,6,7-tetrahydrothieno[2,3-c]pyridine sumo inhibitors and uses thereof | 20200122 |
KR-20070026314-A | Method for in-reaction preparation of chiral compounds derived from oxazaborolidin-borane complexes useful for asymmetric reduction reactions | 20060405 |
CN-1867571-A | In situ preparation of chiral derivatives of oxaborolidine-borane complexes, useful in asymmetric reduction reactions of etheroximes or ketones to chiral alcohols or amines | 20031009 |
DE-602004007947-T2 | METHOD OF IN-SITU-PRODUCING CHIRAL COMPOUNDS DERIVED FROM OXAZABOROLIDINBORO-ADMINISTRATIVE COMPOUNDS USED IN ASYMMETRIC REDUCTION REACTIONS | 20031009 |
EP-1673375-A2 | Method for the in situ preparation of chiral compounds derived from oxazaborolidine-borane complexes, which are used in asymmetric reduction reactions | 20031009 |
Complexity: | 185 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 307.88706 |
Formal Charge: | 0 |
Heavy Atom Count: | 13 |
Hydrogen Bond Acceptor Count: | 2 |
Hydrogen Bond Donor Count: | 0 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 305.8891 |
Rotatable Bond Count: | 3 |
Topological Polar Surface Area: | 26.3 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 3.1 |
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