2,3-Dibromopropene - CAS 513-31-5
Catalog: |
BB027410 |
Product Name: |
2,3-Dibromopropene |
CAS: |
513-31-5 |
Synonyms: |
2,3-dibromoprop-1-ene |
IUPAC Name: | 2,3-dibromoprop-1-ene |
Description: | 2,3-Dibromopropene (CAS# 513-31-5) is a useful research chemical. |
Molecular Weight: | 199.87 |
Molecular Formula: | C3H4Br2 |
Canonical SMILES: | C=C(CBr)Br |
InChI: | InChI=1S/C3H4Br2/c1-3(5)2-4/h1-2H2 |
InChI Key: | YMFWYDYJHRGGPF-UHFFFAOYSA-N |
Boiling Point: | 42-44 °C (17 mmHg) |
Purity: | 98 % |
Density: | 2.13 g/cm3 |
Appearance: | Clear light yellow to brown liquid |
Storage: | Freezer |
MDL: | MFCD00000211 |
LogP: | 2.28990 |
Vapor Pressure: | 7.58 [mmHg] |
GHS Hazard Statement: | H302 (88.89%): Harmful if swallowed [Warning Acute toxicity, oral] |
Precautionary Statement: | P261, P264, P270, P271, P280, P301+P312, P302+P352, P304+P312, P304+P340, P305+P351+P338, P310, P312, P321, P330, P332+P313, P362, P403+P233, P405, and P501 |
Signal Word: | Danger |
Publication Number | Title | Priority Date |
CN-112876434-A | Method for synthesizing 2-vinyl furan by catalyzing furfural and derivatives thereof to convert | 20210208 |
CN-112588316-A | Furan ethylene functional monomer synthesized by catalytic furfuryl alcohol/methanol conversion two-step method and application of catalyst | 20201221 |
CN-112661728-A | Method for synthesizing biomass-based functional monomer based on catalytic conversion of furfuryl alcohol/methanol and application of catalyst | 20201221 |
CN-111320722-A | Special retardation water reducer for secant pile concrete and preparation method thereof | 20200420 |
JP-2021120363-A | Fluorene compounds and polymers thereof and methods for producing them | 20200130 |
PMID | Publication Date | Title | Journal |
17407302 | 20070426 | Formal synthesis of (+/-)-platensimycin | Organic letters |
16526283 | 20060201 | Identification of glutathione conjugates of 2, 3-dibromopropene in male ICR mice | Archives of pharmacal research |
15787564 | 20050401 | Novel carbonyl bromoallylation/Heck reaction sequence. Stereocontrolled access to bicyclic beta-lactams | The Journal of organic chemistry |
15760139 | 20050317 | Synthesis of the eastern portion of ajudazol a based on Stille coupling and double acetylene carbocupration | Organic letters |
14750811 | 20040206 | Straightforward asymmetric entry to highly functionalized 3-substituted 3-hydroxy-beta-lactams via Baylis-Hillman or bromoallylation reactions | The Journal of organic chemistry |
Complexity: | 40.2 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 199.86593 |
Formal Charge: | 0 |
Heavy Atom Count: | 5 |
Hydrogen Bond Acceptor Count: | 0 |
Hydrogen Bond Donor Count: | 0 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 197.86798 |
Rotatable Bond Count: | 1 |
Topological Polar Surface Area: | 0 Å2 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 2.1 |
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