3-Bromo-5-chloropyridine - CAS 73583-39-8
Catalog: |
BB034881 |
Product Name: |
3-Bromo-5-chloropyridine |
CAS: |
73583-39-8 |
Synonyms: |
3-bromo-5-chloropyridine |
IUPAC Name: | 3-bromo-5-chloropyridine |
Description: | 3-Bromo-5-chloropyridine (CAS# 73583-39-8) is a useful research chemical. |
Molecular Weight: | 192.44 |
Molecular Formula: | C5H3BrClN |
Canonical SMILES: | C1=C(C=NC=C1Br)Cl |
InChI: | InChI=1S/C5H3BrClN/c6-4-1-5(7)3-8-2-4/h1-3H |
InChI Key: | BELDOPUBSLPBCQ-UHFFFAOYSA-N |
Boiling Point: | 194.7 °C at 760 mmHg |
Purity: | 98 % |
Density: | 1.736 g/cm3 |
MDL: | MFCD04114221 |
LogP: | 2.49750 |
GHS Hazard Statement: | H301 (86.96%): Toxic if swallowed [Danger Acute toxicity, oral] |
Precautionary Statement: | P261, P264, P270, P271, P280, P301+P310, P302+P352, P304+P340, P305+P351+P338, P310, P312, P321, P330, P332+P313, P337+P313, P362, P403+P233, P405, and P501 |
Signal Word: | Danger |
Publication Number | Title | Priority Date |
WO-2020189540-A1 | Method for preparing aromatic amino acid derivative | 20190315 |
WO-2020135686-A1 | Organic compound with carbazole derivative as core and application thereof to organic electroluminescent device | 20181229 |
WO-2020110008-A1 | Cyclic pentamer compounds as proprotein convertase subtilisin/kexin type 9 (pcsk9) inhibitors for the treatment of metabolic disorder | 20181127 |
WO-2019238628-A1 | Azaindole derivatives as rho- kinase inhibitors | 20180613 |
EP-3807273-A1 | Azaindole derivatives as rho- kinase inhibitors | 20180613 |
Complexity: | 78.8 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 190.91374 |
Formal Charge: | 0 |
Heavy Atom Count: | 8 |
Hydrogen Bond Acceptor Count: | 1 |
Hydrogen Bond Donor Count: | 0 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 190.91374 |
Rotatable Bond Count: | 0 |
Topological Polar Surface Area: | 12.9 Å2 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 2.6 |
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