Skip to Content
Merck
All Photos(2)

Documents

521744

Sigma-Aldrich

2-Amino-6-bromopyridine

98%

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C5H5BrN2
CAS Number:
Molecular Weight:
173.01
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

98%

mp

88-91 °C (lit.)

SMILES string

Nc1cccc(Br)n1

InChI

1S/C5H5BrN2/c6-4-2-1-3-5(7)8-4/h1-3H,(H2,7,8)

InChI key

BKLJUYPLUWUEOQ-UHFFFAOYSA-N

General description

2-Amino- 6-bromopyridine has been synthesized from epichlorohydrin.

Application

2-Amino- 6-bromopyridine may be used in the synthesis of:
  • 2-amino-6-diethylaminopyridine
  • 2,6-di-(methylamino)-pyridine
  • 3-(6-bromopyridin-2-yl)-2-(2,6-difluorophenyl)-1,3-thiazolidin-4-one
  • N-(6-bromopyridin-2-yl)dodecylamide
  • 2-bromo-6-iodopyridine
Employed in an efficient one-pot synthesis of 7-azaindoles.
Used in the synthesis of anti-HIV agents.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

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’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

Slide 1 of 1

1 of 1

Maria Letizia Barreca et al.
Farmaco (Societa chimica italiana : 1989), 58(3), 259-263 (2003-03-07)
This paper reports our work in the field of nonnucleoside RT inhibitors (NNRTIs). On the basis of extensive studies on 1H,3H-thiazolo[3,4-a]benzimidazole derivatives (TBZs) followed by structure-activity relationship (SAR) considerations and molecular modeling, the design and synthesis of a series of
Microwave-assisted synthesis of benzimidazole and thiazolidinone derivatives as HIV-1 RT inhibitors.
Rao A, et al.
ARKIVOC (Gainesville, FL, United States), 147, 155-155 (2004)
Masato Ikeda et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 11(2), 662-668 (2004-11-27)
The bow-shaped molecule 1 bearing a self-complementary DAAD-ADDA (D=donor A=acceptor) hydrogen-bonding array generates, in hydrocarbon solvents, highly ordered supramolecular sheet aggregates that subsequently give rise to gels by formation of an entangled network. The process of hierarchical self-assembly of compound
Synthesis of ?Acetylene-Expanded? Tridentate Ligands
Holmes BT, et al.
Molecules (Basel), 7(5), 447-455 (2002)
II. Derivatives of 2, 6-Diaminopyridine1.
Bernstein J, et al.
Journal of the American Chemical Society, 69(5), 1151-1115 (1947)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service