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经验公式(希尔记法):
C5H5BrN2
化学文摘社编号:
分子量:
173.01
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
产品名称
2-氨基-6-溴吡啶, 98%
InChI
1S/C5H5BrN2/c6-4-2-1-3-5(7)8-4/h1-3H,(H2,7,8)
SMILES string
Nc1cccc(Br)n1
InChI key
BKLJUYPLUWUEOQ-UHFFFAOYSA-N
assay
98%
mp
88-91 °C (lit.)
functional group
bromo
Quality Level
Application
2-氨基-6-溴吡啶可用于以下物质的合成:
- 2-氨基-6-二乙基氨基吡啶
- 2,6-二-(甲基氨基)吡啶
- 3-(6-溴吡啶-2-基)-2-(2,6-二氟苯基)-1,3-噻唑烷-4-酮
- N-(6-溴吡啶-2-基)十二烷基酰胺
- 2-溴-6-碘吡啶
用于合成抗 HIV 试剂。
用于高效一锅法合成 7-氮杂吲哚。
General description
从表氯醇合成了 2-氨基-6-溴吡啶。
hcodes
signalword
Warning
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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)
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