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491047

Sigma-Aldrich

2-(Bromomethyl)pyridine hydrobromide

98%

Synonym(s):

(2-Pyridyl)methyl bromide hydrobromide, 2-Bromomethylpyridine monohydrobromide, 2-Picolyl bromide-hydrobromide

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About This Item

Empirical Formula (Hill Notation):
C6H6BrN · HBr
CAS Number:
Molecular Weight:
252.93
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

98%

mp

149-152 °C (lit.)

SMILES string

Br[H].BrCc1ccccn1

InChI

1S/C6H6BrN.BrH/c7-5-6-3-1-2-4-8-6;/h1-4H,5H2;1H

InChI key

JQDNCGRNPYKRAO-UHFFFAOYSA-N

General description

2-(Bromomethyl)pyridine hydrobromide is a pyridine derivative. It participates in the synthesis of 7-nitrobenz-2-oxa-1,3-diazole (NBD) based colorimetric and fluorescence chemosensor.

Application

2-(Bromomethyl)pyridine hydrobromide may be used in the preparation of :
  • 2-[1-(pyridin-2-ylmethyl)-1H-1,2,3-triazol-4-yl]pyridine
  • 2-morpholin-4-yl-7-(pyridin-2-ylmethoxy)-4H-1,3-benzoxazin-4-one
  • 8-methyl-2-morpholin-4-yl-7-(pyridin-2-ylmethoxy)-4H-1,3-benzoxazin-4-one
  • trans-4-(4-(bis(pyridin-2-ylmethyl)amino)styryl)benzonitrile
  • 2-[N-(2-aminoethanethiol) methyl]-pyridine
  • 2-[N-(ethylenediamino)-methyl]-pyridine
  • 3-(carboxymethyl)-1-[(pyridin-2-yl)methyl]-3H-imidazol-1-ium trifluoroacetate
  • 3-[(S)-1-carboxy-2-methylpropyl]-1-[(pyridin-2-yl)methyl]-3H-imidazol-1-ium trifluoroacetate

Pictograms

Corrosion

Signal Word

Danger

Hazard Statements

Hazard Classifications

Skin Corr. 1B

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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A multicomponent CuAAC ?click? approach to a library of hybrid polydentate 2-pyridyl-1,2,3-triazole ligands: new building blocks for the generation of metallosupramolecular architectures.
Crowley JD and Bandeen PH.
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A number of new 2-amino-[5, 6, 7 and 8]-O-substituted 1,3-benzoxazines, and 2-amino 8-methyl-7-O-substituted-1,3-benzoxazines were synthesized. Thirty one new compounds were tested for their effect on collagen induced platelet aggregation and it was found that the most active compounds were 8-methyl-2-morpholin-4-yl-7-(pyridin-3-ylmethoxy)-4H-1,3-benzoxazin-4-one

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