1. Home
  2. 3-Bromo-4-(chloromethyl)pyridine Hydrochloride

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)-

3-Bromo-4-(chloromethyl)pyridine Hydrochloride

ClCc1ccncc1Br.Cl Request for Quotation
Chemical Name: 3-Bromo-4-(chloromethyl)pyridine Hydrochloride
CAS Number: 1418117-80-2
Product Number: AG001H83(AGN-PC-0WA86T)
Synonyms:
MDL No: MFCD22682795
Molecular Formula: C6H6BrCl2N
Molecular Weight: 242.9285

Identification/Properties

Properties
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
242.93g/mol
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
1
Exact Mass:
240.90607g/mol
Monoisotopic Mass:
240.90607g/mol
Topological Polar Surface Area:
12.9Ų
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
89.1
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:
2
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Danger
UN#:
1759
Hazard Statements:
H315-H318-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
8
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


3-Bromo-4-(chloromethyl)pyridine Hydrochloride is a versatile chemical compound commonly used in organic synthesis applications. Due to its unique structure and reactivity, this compound serves as a valuable building block in the creation of diverse organic molecules. In chemical synthesis, 3-Bromo-4-(chloromethyl)pyridine Hydrochloride can participate in various reactions to introduce functional groups or modify existing molecular backbones. Its bromine and chlorine substituents confer different properties and allow for selective derivatization. This compound can be used as a precursor in the synthesis of pharmaceuticals, agrochemicals, or other specialty chemicals where precise control over the final molecular structure is essential. Additionally, its pyridine core imparts specific chemical reactivity that can be harnessed in designing complex molecular architectures.The application of 3-Bromo-4-(chloromethyl)pyridine Hydrochloride in chemical synthesis extends to the development of advanced materials, catalysts, and bioactive compounds. By incorporating this compound into synthetic pathways, chemists can access a wide array of functionalized products with tailored properties for targeted applications in various industries.