2,6-Dibromopyridine - CAS 626-05-1
Catalog: |
BB031685 |
Product Name: |
2,6-Dibromopyridine |
CAS: |
626-05-1 |
Synonyms: |
2,6-dibromopyridine |
IUPAC Name: | 2,6-dibromopyridine |
Description: | 2,6-Dibromopyridine (CAS# 626-05-1) is used as a starting material to synthesize 2,2'-bipyridines (such as 5-Cyano-1,6-dihydro-6-oxo-[3,4'-bipyridine]-2-carboxylic Acid [C979150]) via a Stille-type cross-coupling reaction. 2,6-Dibromopyridine is also used as a reagent to synthesize pyridylpyrimidine fungicides, compounds that eliminate fungi by cycling copper through the cell membrane, where it reaches toxic levels. |
Molecular Weight: | 236.89 |
Molecular Formula: | C5H3Br2N |
Canonical SMILES: | C1=CC(=NC(=C1)Br)Br |
InChI: | InChI=1S/C5H3Br2N/c6-4-2-1-3-5(7)8-4/h1-3H |
InChI Key: | FEYDZHNIIMENOB-UHFFFAOYSA-N |
Boiling Point: | 255 °C |
Melting Point: | 118-119 °C |
Purity: | 96 % |
Density: | 2.059 g/cm3 |
Appearance: | White to light yellow crystalline powder |
Storage: | Keep container closed when not in use. Store in a tightly closed container. Store in a cool, dry, well-ventilated area away from incompatible substances. |
MDL: | MFCD00006223 |
LogP: | 2.60660 |
GHS Hazard Statement: | H300 (96.43%): Fatal if swallowed [Danger Acute toxicity, oral] |
Precautionary Statement: | P261, P264, P270, P271, P273, P280, P301+P310, P302+P352, P304+P312, P304+P340, P305+P351+P338, P312, P321, P330, P332+P313, P337+P313, P362, P403+P233, P405, and P501 |
Signal Word: | Danger |
Publication Number | Title | Priority Date |
CN-113045602-A | Pyridine dibenzylamine-containing fourth subgroup metal complex and application thereof | 20210311 |
CN-112774734-A | Copper catalyst for synthesizing quinoline compound and preparation method thereof | 20210222 |
CN-112958161-A | Palladium catalyst and application thereof in catalyzing aryl ethanol compound deoxidation coupling reaction | 20210222 |
CN-112958162-A | Palladium catalyst for catalyzing quinazolinone synthesis and olefination reaction | 20210222 |
CN-113024548-A | Process for preparing 2-amino-9H-pyridine [2,3-b ] indole | 20210129 |
PMID | Publication Date | Title | Journal |
22968972 | 20121022 | Rotation-locked 2,6-pyrido-allenophanes: characterization of all stereoisomers | Chemistry (Weinheim an der Bergstrasse, Germany) |
21222493 | 20110204 | Synthesis of di-, tri-, and tetrasulfides through multifold carbon-sulfur cross-coupling reactions with indium tri(organothiolates) in a one-pot procedure | The Journal of organic chemistry |
21589141 | 20101031 | Dimethyl 4,4'-(pyridine-2,6-diyl)dibenzoate | Acta crystallographica. Section E, Structure reports online |
18270986 | 20080101 | Concise total synthesis of the thiazolyl peptide antibiotic GE2270 A | Chemistry (Weinheim an der Bergstrasse, Germany) |
16847994 | 20061213 | Methylazacalixpyridines: remarkable bridging nitrogen-tuned conformations and cavities with unique recognition properties | Chemistry (Weinheim an der Bergstrasse, Germany) |
Complexity: | 68.8 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 236.86117 |
Formal Charge: | 0 |
Heavy Atom Count: | 8 |
Hydrogen Bond Acceptor Count: | 1 |
Hydrogen Bond Donor Count: | 0 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 234.86322 |
Rotatable Bond Count: | 0 |
Topological Polar Surface Area: | 12.9 Å2 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 2.9 |
Online Inquiry
Customer Support
Customer Centered
Related Functional Groups
Pyridines
Customers Also Viewed
INDUSTRY LEADERS TRUST OUR PRODUCTS