2,3-Bis(bromomethyl)quinoxaline - CAS 3138-86-1
Catalog: |
BB020903 |
Product Name: |
2,3-Bis(bromomethyl)quinoxaline |
CAS: |
3138-86-1 |
Synonyms: |
2,3-bis(bromomethyl)quinoxaline |
IUPAC Name: | 2,3-bis(bromomethyl)quinoxaline |
Description: | 2,3-Bis(bromomethyl)quinoxaline (CAS# 3138-86-1) is a useful research chemical compound. |
Molecular Weight: | 315.99 |
Molecular Formula: | C10H8Br2N2 |
Canonical SMILES: | C1=CC=C2C(=C1)N=C(C(=N2)CBr)CBr |
InChI: | InChI=1S/C10H8Br2N2/c11-5-9-10(6-12)14-8-4-2-1-3-7(8)13-9/h1-4H,5-6H2 |
InChI Key: | LHKFFORGJVELPC-UHFFFAOYSA-N |
Boiling Point: | 345.7 °C at 760 mmHg |
Density: | 1.869 g/cm3 |
Appearance: | Grey to brown powder or crystals |
MDL: | MFCD00006729 |
LogP: | 3.41960 |
GHS Hazard Statement: | H314 (100%): Causes severe skin burns and eye damage [Danger Skin corrosion/irritation] |
Precautionary Statement: | P260, P261, P264, P271, P280, P301+P330+P331, P303+P361+P353, P304+P340, P305+P351+P338, P310, P312, P321, P363, P403+P233, P405, and P501 |
Signal Word: | Danger |
Publication Number | Title | Priority Date |
WO-2019179985-A1 | Inhibitors of mint and uses thereof | 20180319 |
CN-108358997-A | A kind of stabilization polypeptide that intracellular that modifying construction of strategy using double sulfosalts is reversible | 20180301 |
WO-2019096907-A1 | Aryl annulated macrocyclic indole derivatives | 20171117 |
EP-3710447-A1 | Aryl annulated macrocyclic indole derivatives | 20171117 |
US-2021253598-A1 | Aryl annulated macrocyclic indole derivatives | 20171117 |
PMID | Publication Date | Title | Journal |
22245018 | 20120401 | Synthesis and antimicrobial activity of 2,3-bis(bromomethyl)quinoxaline derivatives | Bioorganic chemistry |
21879091 | 20111107 | Synthesis and characterization of diiron dithiolate complexes containing a quinoxaline bridge | Dalton transactions (Cambridge, England : 2003) |
17407354 | 20070427 | An improved understanding of the reaction of bis(bromomethyl)quinoxaline 1-N-oxides with amines using substituent effects | The Journal of organic chemistry |
15960505 | 20050624 | Controlling the outcome of an N-alkylation reaction by using N-oxide functional groups | The Journal of organic chemistry |
Complexity: | 169 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 315.90337 |
Formal Charge: | 0 |
Heavy Atom Count: | 14 |
Hydrogen Bond Acceptor Count: | 2 |
Hydrogen Bond Donor Count: | 0 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 313.90542 |
Rotatable Bond Count: | 2 |
Topological Polar Surface Area: | 25.8 Å2 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 2.4 |
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