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2,6-Bis(bromomethyl)pyridine, 98%|218208|7703-74-4

2,6-Bis(bromomethyl)pyridine, 98%

Cat. No JK218208_1_G
J&K Chemical

Product Information

Product Name
2,6-Bis(bromomethyl)pyridine, 98%
Brand Name
J&K
Product Number
218208
CAS
7703-74-4
Molecular Formula
C7H7Br2N
Molecular Weight
264.95
SDS Document
View/Download
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
603610
IUPAC Name
2,6-bis(bromomethyl)pyridine
InChI Key
QUTSYCOAZVHGGT-UHFFFAOYSA-N
SMILES
C1=CC(=NC(=C1)CBr)CBr

Properties

Melting Point
85-87

Safety Information

GHS Symbols
Hazard Symbol
Signal Word
Warning
Hazard Statement
H302
H315
H319
H335
Precautionary Statement
P270
P330
P501
P280
P321
P261
P271
P319
P405
P301+P317
P302+P352
P332+P317
P362+P364
P264+P265
P305+P351+P338
P337+P317
P304+P340
P403+P233

References Data Source From Pubchem

Development of a 177Lu-labeled EphA2-targeting cyclic peptide combined with an HPK1 inhibitor for synergistic anti-tumor effects
Publication Name: Cellular oncology (Dordrecht, Netherlands)
Publication Date: 2025-10-02
DOI: 10.1007/s13402-025-01105-1

Macrocyclic β-arch peptides that mimic the structure and function of disease-associated tau folds
Publication Name: Nature Chemistry
Publication Date: 2025-04-30
DOI: 10.1038/s41557-025-01805-z

Slowing the reactivity of dicyclometalated Pd(II) complexes through the 2,6-bis(N-heterocyclic carbene)pyridine (C^N^C) non-leaving ligands: kinetic and computational study
Publication Name: Transition Metal Chemistry
Publication Date: 2024-08-21
DOI: 10.1007/s11243-024-00601-x

C(sp3)–C(sp3) bond formation through nitrogen deletion of secondary amines using O-diphenylphosphinylhydroxylamine
Publication Name: Nature Synthesis
Publication Date: 2024-06-07
DOI: 10.1038/s44160-024-00559-9

eTFC-01: a dual-labeled chelate-bridged tracer for SSTR2-positive tumors
Publication Name: EJNMMI Radiopharmacy and Chemistry
Publication Date: 2024-05-22
DOI: 10.1186/s41181-024-00272-0

2,6-Bis(bromomethyl)pyridine, 98%

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