2-Bromoquinoline - CAS 2005-43-8
Catalog: |
BB015480 |
Product Name: |
2-Bromoquinoline |
CAS: |
2005-43-8 |
Synonyms: |
2-bromoquinoline |
IUPAC Name: | 2-bromoquinoline |
Description: | 2-Bromoquinoline (CAS# 2005-43-8) is a useful research chemical. |
Molecular Weight: | 208.05 |
Molecular Formula: | C9H6BrN |
Canonical SMILES: | C1=CC=C2C(=C1)C=CC(=N2)Br |
InChI: | InChI=1S/C9H6BrN/c10-9-6-5-7-3-1-2-4-8(7)11-9/h1-6H |
InChI Key: | QKJAZPHKNWSXDF-UHFFFAOYSA-N |
Boiling Point: | 292.5 °C at 760 mmHg |
Purity: | 98 % |
Density: | 1.564 g/cm3 |
MDL: | MFCD00234480 |
LogP: | 2.99730 |
GHS Hazard Statement: | H302 (84.44%): Harmful if swallowed [Warning Acute toxicity, oral] |
Precautionary Statement: | P261, P264, P270, P271, P280, P301+P312, P302+P352, P304+P340, P305+P351+P338, P310, P312, P321, P330, P332+P313, P337+P313, P362, P403+P233, P405, and P501 |
Signal Word: | Danger |
Publication Number | Title | Priority Date |
CN-112979619-A | Method for catalyzing dehydrogenation coupling reaction of nitrogen heteroaromatic ring compound and cyclic ether by using Bronsted acid | 20210128 |
CN-112409253-A | Method for synthesizing chiral alpha-tertiary amine by catalytic kinetic resolution | 20201127 |
CN-112175006-A | Preparation method of pyridine diphenylphosphine derivative | 20201110 |
CN-112390751-A | Toll-like receptor-7 small molecule inhibitor and preparation method thereof | 20201105 |
CN-112239452-A | Electron transport type heteroanthracene derivative and organic electroluminescent device thereof | 20201014 |
PMID | Publication Date | Title | Journal |
22890246 | 20121021 | A highly efficient and aerobic protocol for the synthesis of N-heteroaryl substituted 9-arylcarbazolyl derivatives via a palladium-catalyzed ligand-free Suzuki reaction | Organic & biomolecular chemistry |
22364416 | 20120308 | Identification, design and biological evaluation of bisaryl quinolones targeting Plasmodium falciparum type II NADH:quinone oxidoreductase (PfNDH2) | Journal of medicinal chemistry |
22364417 | 20120308 | Identification, design and biological evaluation of heterocyclic quinolones targeting Plasmodium falciparum type II NADH:quinone oxidoreductase (PfNDH2) | Journal of medicinal chemistry |
21270126 | 20110401 | Combined X-ray, NMR, and kinetic analyses reveal uncommon binding characteristics of the hepatitis C virus NS3-NS4A protease inhibitor BI 201335 | The Journal of biological chemistry |
Complexity: | 138 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 206.96836 |
Formal Charge: | 0 |
Heavy Atom Count: | 11 |
Hydrogen Bond Acceptor Count: | 1 |
Hydrogen Bond Donor Count: | 0 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 206.96836 |
Rotatable Bond Count: | 0 |
Topological Polar Surface Area: | 12.9 Å2 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 2.8 |
-
Catalog: BB001559
(3-methoxyquinolin-6-yl)methanol
Detail
-
Catalog: BB004090
(3-Pyridyl)(3-quinolyl)methanol
Detail
-
Catalog: BB032144
(R)-2-Methyl-1,2,3,4-tetrahydroquinoline
Detail
-
Catalog: BB028529
1-(3,4-Dihydroisoquinolin-2(1H)-yl)propan-2-amine
Detail
-
Catalog: BB008062
(S)-3-(1-Aminoethyl)-8-chloro-2-phenylisoquinolin-1(2H)-one
Detail
-
Catalog: BB010597
(R)-1,2,3,4-Tetrahydroisoquinoline-1-carboxylic Acid
Detail
-
Catalog: BB043168
(+/-)-3-Amino-1,2,3,4-tetrahydroquinoline
Detail
-
Catalog: BB023177
(Phenyl)(3-quinolyl)methanol
Detail
Online Inquiry
Customer Support
Customer Centered
Related Functional Groups
Quinoline/Isoquinoline
Customers Also Viewed
INDUSTRY LEADERS TRUST OUR PRODUCTS