It is a heterocyclic building block for the synthesis of a variety of pyridine derivatives. It coordinates with metal ions through N-atom to form complexes. The conformational flexibility of the bromomethyl arms makes it an ideal choice for the generation of macrocycles. 2,6-bis(chloromethyl)pyridine crystals are monoclinic with space group P21/c. Its synthesis has been reported. The FT-IR and FT-Raman spectra of 2,6-bis(chloromethyl)pyridine (BCMP) have been recorded in the regions 4000-400cm-1 and 3500-100cm-1, respectively.It may be used in the following studies: . Synthesis of a sensitive fluorescent chemosensor for Hg2+, composed of two aminonaphthalimide fluorophores and a receptor of 2,6-bis(aminomethyl)pyridine. . Preparation of carbene pincer ligands, required for the preparation of palladium pincer carbene complex. . Synthesis of 2-(di-tert-butylphosphinomethyl)-6-diethylaminomethyl)pyridine, PNN ligand.
Specifications and Purity: ≥98%
MDL Number: MFCD00142844
Molecular Formula: C7H7Cl2N
Molecular Weight: 176.04
PubChem CID: 316654
Isomeric SMILES: C1=CC(=NC(=C1)CCl)CCl
Beilstein Registry Number: 116355
Related Documents: https://ald-pub-files.oss-cn-shanghai.aliyuncs.com/aladdinsci/pdp/sds/1/B151850-SCI_ccdfff5607db5f3234bbf8f2460217e5.pdf
- UPC:
- 51101907
- Condition:
- New
- HazmatClass:
- No
- WeightUOM:
- LB
- MPN:
- B151850-5g
- CAS:
- 3099-28-3
- Product Size:
- 5g
- Hazard Statement Codes:
- H314
- Precautionary Statement Codes:
- P280:P264
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