1. Home
  2. Pyridine, 2,3,5-tribromo-

Contact Angene

Tel: +852 8191 6999

Email: sales@angenechemical.com

Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

Pyridine, 2,3,5-tribromo-

Brc1cnc(c(c1)Br)Br Request for Quotation
Chemical Name: Pyridine, 2,3,5-tribromo-
CAS Number: 75806-85-8
Product Number: AG005UHZ(AGN-PC-0JU1XH)
Synonyms:
MDL No:
Molecular Formula: C5H2Br3N
Molecular Weight: 315.7881

Identification/Properties

Properties
MP:
44.0 to 48.0 °C
BP:
280.2°C at 760 mmHg
Storage:
Room Temperature;Inert atmosphere;
Form:
Solid
Computed Properties
Molecular Weight:
315.79g/mol
XLogP3:
3.3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
314.772g/mol
Monoisotopic Mass:
312.774g/mol
Topological Polar Surface Area:
12.9A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
98.2
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


2,3,5-Tribromopyridine is a valuable chemical compound commonly used in chemical synthesis due to its unique properties and versatile applications. Its bromine substituents make it an excellent building block for various organic reactions and transformations. In organic synthesis, 2,3,5-Tribromopyridine can serve as a halogenation reagent to introduce bromine atoms onto other molecules, allowing for the formation of new carbon-carbon and carbon-heteroatom bonds. This compound is particularly useful in the preparation of complex pharmaceuticals, agrochemicals, and materials with specific functionalities. Additionally, 2,3,5-Tribromopyridine can participate in various cross-coupling reactions, such as Suzuki, Heck, and Stille couplings, to create biaryl compounds or functionalized heterocycles. Its ability to undergo multiple transformations makes it a versatile tool in the synthesis of highly sought-after organic molecules. Furthermore, the presence of multiple bromine atoms in 2,3,5-Tribromopyridine provides opportunities for further derivatization, enabling the synthesis of structurally diverse compounds with tailored properties. Its applications extend beyond organic synthesis to materials science, catalysis, and pharmaceutical research, highlighting its importance as a key reagent in modern chemical synthesis strategies.