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491748

Sigma-Aldrich

4-(Bromomethyl)pyridine hydrobromide

97%

Synonym(s):

(4-Pyridyl)methyl bromide hydrobromide, 4-(Bromomethyl)pyridine monohydrobromide, 4-Picolyl bromide hydrobromide

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About This Item

Empirical Formula (Hill Notation):
C6H6BrN · HBr
CAS Number:
73870-24-3
Molecular Weight:
252.93
MDL number:
MFCD01863545
UNSPSC Code:
12352100
PubChem Substance ID:
24872681
NACRES:
NA.22

Quality Level

100

Assay

97%

mp

189-192 °C (lit.)

functional group

bromo

SMILES string

Br[H].BrCc1ccncc1

InChI

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

InChI key

VAJUUDUWDNCECT-UHFFFAOYSA-N

Related Categories

General description

4-(Bromomethyl)pyridine hydrobromide is a substituted pyridine. It reacts with 1,2-ethanediamine and 1,3-propanediamine to form the corresponding diamines.

Application

4-(Bromomethyl)pyridine hydrobromide may be used in the preparation of:
  • 3-(4-pyridylmethyl)-2′,3′-di-O-oleyl-5′-O-(4,4′-dimethoxytriphenylmethyl)uridine
  • 3-(4-pyridylmethyl)-3′-O-oleyl-5′-O-(4,4-dimethoxytriphenylmethyl)-thymidine
  • 1,4-bis(N-hexyl-4-pyridinium)butadiene diperchlorate
It may also be used in the preparation of the following benzoxazine derivatives:
  • 2-morpholin-4-yl-7-(pyridin-4-ylmethoxy)-4H-1,3-benzoxazin-4-one
  • 8-methyl-2-morpholin-4-yl-7-(pyridin-4-ylmethoxy)-4H-1,3-benzoxazin-4-one
  • 2-morpholin-4-yl-8-(pyridin-4-ylmethoxy)-4H-1,3-benzoxazin-4-one

Pictograms

Corrosion
GHS05

Signal Word

Danger

Hazard Statements

H314

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

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Certificates of Analysis (COA)

Lot/Batch Number
MKCS2653
MKBV9025V
MKBH6507V
MKBH9291V
MKBB0639

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Luca Simeone et al.
Molecular bioSystems, 7(11), 3075-3086 (2011-09-08)
Novel thymidine- or uridine-based nucleolipids, containing one hydrophilic oligo(ethylene glycol) chain and one or two oleic acid residues (called ToThy, HoThy and DoHu), have been synthesized with the aim to develop bio-compatible nanocarriers for drug delivery and/or produce pro-drugs. Microstructural
Photoinduced electron transfer in supramolecular complexes of a p-extended viologen with porphyrin monomer and dimer.
Fukuzumi S, et al.
Royal Society of Chemistry Advances, 2(9), 3741-3747 (2012)
Cristiane F da Costa et al.
Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie, 63(1), 40-42 (2008-02-12)
We report in this work the preparation and the in vitro antileishmanial activity of a series of long chains N-monoalkylated diamines and two pyridinediamine derivatives. Several compounds, tested for their in vitro antiproliferative activity against Leishmania amazonensis and Leishmania chagasi
Saleh Ihmaid et al.
European journal of medicinal chemistry, 45(11), 4934-4946 (2010-08-31)
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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