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2-Bromopyridine

CAS No.:
109-04-6
Catalog Number:
AG00336Y
Molecular Formula:
C5H4BrN
Molecular Weight:
157.9960
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
5g
98%(GC)
In Stock USA
United States
$37
- +
25g
98%(GC)
In Stock USA
United States
$43
- +
100g
98%(GC)
In Stock USA
United States
$76
- +
250g
98%(GC)
In Stock USA
United States
$132
- +
Product Description
Catalog Number:
AG00336Y
Chemical Name:
2-Bromopyridine
CAS Number:
109-04-6
Molecular Formula:
C5H4BrN
Molecular Weight:
157.9960
MDL Number:
MFCD00006219
IUPAC Name:
2-bromopyridine
InChI:
InChI=1S/C5H4BrN/c6-5-3-1-2-4-7-5/h1-4H
InChI Key:
IMRWILPUOVGIMU-UHFFFAOYSA-N
SMILES:
Brc1ccccn1
EC Number:
203-641-6
UNII:
7Z7MLC4VD8
NSC Number:
8031
Properties
Complexity:
56  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
156.953g/mol
Formal Charge:
0
Heavy Atom Count:
7  
Hydrogen Bond Acceptor Count:
1  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
157.998g/mol
Monoisotopic Mass:
156.953g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
12.9A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
1.4  
Literature
Title Journal
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8-Azatetracyclines: synthesis and evaluation of a novel class of tetracycline antibacterial agents. Journal of medicinal chemistry 20110310
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Mixed effect of the supporting electrolyte and the zinc anode in the electrochemical homocoupling of 2-bromopyridines catalyzed by nickel complexes in an undivided cell. The Journal of organic chemistry 20051223
Improved synthesis of aryltrialkoxysilanes via treatment of aryl Grignard or lithium reagents with tetraalkyl orthosilicates. The Journal of organic chemistry 20041126
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Siloxane-based cross-coupling of bromopyridine derivatives: studies for the synthesis of streptonigrin and lavendamycin. Organic letters 20031211
Electrophilic terminal phosphinidene complex-Lewis base adducts: chemistry between carbon-halide bond activation and weak Lewis base adduct formation. Chemical communications (Cambridge, England) 20031207
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Mode of action and quantitative structure-activity correlations of tuberculostatic drugs of the isonicotinic acid hydrazide type. Journal of medicinal chemistry 19760401
Properties