Introduction:Basic information about CAS 52200-48-3|3-Bromo-2-chloropyridine, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
3-Bromo-2-chlorolpyridine is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
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Research Areas >>Others
Chemical & Physical Properties
Density
1.7±0.1 g/cm3
Boiling Point
219.8±20.0 °C at 760 mmHg
Melting Point
54-57 °C(lit.)
Molecular Formula
C5H3BrClN
Molecular Weight
192.44
Flash Point
86.8±21.8 °C
Exact Mass
190.913727
PSA
12.89000
LogP
2.33
Vapour Pressure
0.2±0.4 mmHg at 25°C
Index of Refraction
1.581
InChIKey
HDYNIWBNWMFBDO-UHFFFAOYSA-N
SMILES
Clc1ncccc1Br
Safety Information
Symbol
GHS07
Signal Word
Warning
Hazard Statements
H315-H319-H335
Precautionary Statements
P261-P305 + P351 + P338
Personal Protective Equipment
dust mask type N95 (US);Eyeshields;Gloves
Hazard Codes
Xi:Irritant;
Risk Phrases
R36/37/38
Safety Phrases
S26-S36-S37/39
RIDADR
NONH for all modes of transport
WGK Germany
3
HS Code
2933399090
Customs
HS Code
2933399090
Summary
2933399090. other compounds containing an unfused pyridine ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%
Articles5
More Articles
An efficient two-step total synthesis of the quaterpyridine nemertelline.
J. Org. Chem. 68(26) , 10178-80, (2003)
Regioselective and univocal Suzuki cross-coupling reactions performed on halopyridinyl boronic acids provide a flexible and versatile route to a multigram scale synthesis of 2,2'-dichloro-3,4'-bipyrid...
Synthesis and antimicrobial activity studies of ortho-chlorodiarylamines and heteroaromatic tetracyclic systems in the benzo[b]thiophene series.
Bioorg. Med. Chem. 14(20) , 6827-31, (2006)
ortho-Chlorodiarylamines in the 2,3,7-trimethylbenzo[b]thiophene series were prepared in high yields (70-85%) by C-N palladium-catalyzed cross-coupling using P(t-Bu)(3) as ligand and NaOt-Bu as base. ...
Synthesis of novel halopyridinylboronic acids and esters. Part 2: 2, 4, or 5-Halopyridin-3-yl-boronic acids and esters. Bouillon A, et al.