1,4-Dibromo-2,3-butanedione - CAS 6305-43-7
Catalog: |
BB031968 |
Product Name: |
1,4-Dibromo-2,3-butanedione |
CAS: |
6305-43-7 |
Synonyms: |
1,4-dibromobutane-2,3-dione |
IUPAC Name: | 1,4-dibromobutane-2,3-dione |
Description: | 1,4-Dibromo-2,3-butanedione (CAS# 6305-43-7) is a useful research chemical compound. |
Molecular Weight: | 243.88 |
Molecular Formula: | C4H4Br2O2 |
Canonical SMILES: | C(C(=O)C(=O)CBr)Br |
InChI: | InChI=1S/C4H4Br2O2/c5-1-3(7)4(8)2-6/h1-2H2 |
InChI Key: | RZMOICJDRADLCT-UHFFFAOYSA-N |
Boiling Point: | 213 °C at 760 mmHg |
Density: | 2.117 g/cm3 |
Appearance: | Light yellow powder |
MDL: | MFCD00000205 |
LogP: | 0.91440 |
GHS Hazard Statement: | H315 (90.48%): Causes skin irritation [Warning Skin corrosion/irritation] |
Precautionary Statement: | P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501 |
Signal Word: | Warning |
Publication Number | Title | Priority Date |
CN-112778206-A | Preparation method and application of high-absorption chrome tanning auxiliary agent containing ketosulfonate structure | 20210107 |
CN-112452325-A | Catalyst for preparing 1, 3-butanediol by hydrogenating 3-hydroxybutyraldehyde, and preparation method and application thereof | 20201126 |
CN-112250587-A | Tetraphenylbenzene-based heterogeneous covalent organic framework material and preparation method thereof | 20201016 |
JP-2021154291-A | Solder Compositions for Laser Soldering, Electronic Substrates, and Methods for Manufacturing Electronic Substrates | 20200325 |
WO-2021150574-A1 | Sulfonimidamide compounds as nlrp3 modulators | 20200122 |
PMID | Publication Date | Title | Journal |
20490291 | 20090501 | Synthesis, Antiinflammatory and HIV-1 Integrase Inhibitory Activities of 1,2-Bis[5-thiazolyl]ethane-1,2-dione Derivatives | Indian journal of pharmaceutical sciences |
19333470 | 20090421 | Diastereoselective formation of a dicopper(i) helicate with a chiral tetradentate pyridylthiazole ligand | Chemical communications (Cambridge, England) |
11955000 | 20020201 | A new nonhydrolyzable reactive cAMP analog, (Sp)-adenosine-3',5'-cyclic-S-(4-bromo-2,3-dioxobutyl)monophosphorothioate irreversibly inactivates human platelet cGMP-inhibited cAMP phosphodiesterase | Bioorganic chemistry |
Complexity: | 96.6 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 243.85576 |
Formal Charge: | 0 |
Heavy Atom Count: | 8 |
Hydrogen Bond Acceptor Count: | 2 |
Hydrogen Bond Donor Count: | 0 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 241.85780 |
Rotatable Bond Count: | 3 |
Topological Polar Surface Area: | 34.1 Å2 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 1.2 |
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