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Home Halogens 2,6-Dibromopyridine

2,6-Dibromopyridine

CAS No.:
626-05-1
Catalog Number:
AG003311
Molecular Formula:
C5H3Br2N
Molecular Weight:
236.8920
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
1g
98%
In Stock USA
United States
$13
- +
25g
98%
In Stock USA
United States
$38
- +
100g
98%(HPLC)
In Stock USA
United States
$112
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500g
98%(HPLC)
In Stock USA
United States
$321
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Product Description
Catalog Number:
AG003311
Chemical Name:
2,6-Dibromopyridine
CAS Number:
626-05-1
Molecular Formula:
C5H3Br2N
Molecular Weight:
236.8920
MDL Number:
MFCD00006223
IUPAC Name:
2,6-dibromopyridine
InChI:
InChI=1S/C5H3Br2N/c6-4-2-1-3-5(7)8-4/h1-3H
InChI Key:
FEYDZHNIIMENOB-UHFFFAOYSA-N
SMILES:
Brc1cccc(n1)Br
EC Number:
210-926-9
NSC Number:
613
Properties
Complexity:
68.8  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
236.861g/mol
Formal Charge:
0
Heavy Atom Count:
8  
Hydrogen Bond Acceptor Count:
1  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
236.894g/mol
Monoisotopic Mass:
234.863g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
12.9A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
2.9  
Literature
Title Journal
Rotation-locked 2,6-pyrido-allenophanes: characterization of all stereoisomers. Chemistry (Weinheim an der Bergstrasse, Germany) 20121022
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 20110204
Dimethyl 4,4'-(pyridine-2,6-diyl)dibenzoate. Acta crystallographica. Section E, Structure reports online 20101101
Concise total synthesis of the thiazolyl peptide antibiotic GE2270 A. Chemistry (Weinheim an der Bergstrasse, Germany) 20080101
Design, synthesis, and crystal structure of selective 2-pyridone tissue factor VIIa inhibitors. Journal of medicinal chemistry 20031023
Synthesis of a muscarinic receptor antagonist via a diastereoselective Michael reaction, selective deoxyfluorination and aromatic metal-halogen exchange reaction. The Journal of organic chemistry 20011005
Properties