추천 제품
분석
98%
refractive index
n20/D 1.625 (lit.)
bp
140-146 °C/15 mmHg (lit.)
mp
18-20 °C (lit.)
density
1.15 g/mL at 20 °C (lit.)
SMILES string
COc1ccc2ncccc2c1
InChI
1S/C10H9NO/c1-12-9-4-5-10-8(7-9)3-2-6-11-10/h2-7H,1H3
InChI key
HFDLDPJYCIEXJP-UHFFFAOYSA-N
유전자 정보
human ... CYP2D6(1565)
유사한 제품을 찾으십니까? 방문 제품 비교 안내
관련 카테고리
애플리케이션
6-Methoxyquinoline is used as a precursor in the synthesis of:
- Fluorescent zinc and chlorine sensors.
- 5-Amino-2-aroylquinolines as potent tubulin polymerization inhibitors.
- 3-Fluoro-6-methoxyquinoline derivatives as inhibitors of bacterial DNA gyrase and topoisomerase.
- Cobalt-based ternary metal-organic complex as single?ion magnets.
신호어
Warning
유해 및 위험 성명서
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2
Storage Class Code
10 - Combustible liquids
WGK
WGK 3
Flash Point (°F)
>230.0 °F
Flash Point (°C)
> 110 °C
개인 보호 장비
Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)
시험 성적서(COA)
제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.
이미 열람한 고객
Journal of chromatography. A, 1269, 262-269 (2012-08-28)
The determination of trace amounts of d-amino acids (d-AAs) even in tissue samples of higher developed animals, mammals and humans has opened a wide field of biological questions to be investigated. d-Ala, d-Asp and d-Ser have already been identified to
Novel 3-fluoro-6-methoxyquinoline derivatives as inhibitors of bacterial DNA gyrase and topoisomerase IV.
Bioorganic & Medicinal Chemistry Letters, 27(15), 3353-3358 (2017)
Single-Ion Magnets Based on Mononuclear Cobalt (II) Complexes with Sulfadiazine.
European Journal of Inorganic Chemistry, 2016(29), 4835-4841 (2016)
Analytical chemistry, 78(9), 3133-3137 (2006-04-29)
Human neutrophils synthesize hypochlorous acid, a nonradical oxidant, as one of the antimicrobial agents to kill phagocytosed pathogens within phagolysosomes. The production of HOCl is catalyzed by myeloperoxidase using chloride anions (Cl-). Even though various approaches have been documented to
5-Amino-2-aroylquinolines as highly potent tubulin polymerization inhibitors. Part 2. The impact of bridging groups at position C-2.
Journal of Medicinal Chemistry, 54(24), 8517-8525 (2011)
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