추천 제품
분석
97%
형태
solid
mp
172-176 °C (lit.)
SMILES string
OC(=O)c1ccc(F)cc1Br
InChI
1S/C7H4BrFO2/c8-6-3-4(9)1-2-5(6)7(10)11/h1-3H,(H,10,11)
InChI key
RRKPMLZRLKTDQV-UHFFFAOYSA-N
유사한 제품을 찾으십니까? 방문 제품 비교 안내
일반 설명
Amination of 2-bromo-4-fluorobenzoic acid with aniline is reported to yield N-phenyl-4-fluoro-anthranilic acid.
애플리케이션
2-Bromo-4-fluorobenzoic acid may be used in the synthesis of:
- 3-fluoro-8-(methylthio)dibenzo[b,f]thiepin-10(11H)-one
- 2-fluoro-8-(methylthio)dibenzo[b,f]thiepin-10(11H)-one
- 2-((2-carboxy-5-fluorophenyl)amino)-3-methoxybenzoic acid
- 2-bromo-4-fluorobenzamide
신호어
Warning
유해 및 위험 성명서
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
표적 기관
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
dust mask type N95 (US), Eyeshields, Gloves
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.
Neuroleptics with protracted action: 3-Fluoro derivatives of methiothepin and oxyprothepin and their 2-fluoro analogues.
Collection of Czechoslovak Chemical Communications, 40(11), 3519-3529 (1975)
Bioorganic & medicinal chemistry, 19(7), 2190-2198 (2011-03-23)
Aim of this study was to label the potent dual P-glycoprotein (Pgp) and breast cancer resistance protein (BCRP) inhibitor elacridar (1) with (18)F to provide a positron emission tomography (PET) radiotracer to visualize Pgp and BCRP. A series of new
Organic & biomolecular chemistry, 9(7), 2233-2239 (2011-02-08)
A Heck cyclisation approach is described for the rapid synthesis of a library of natural product-like small molecules, based on the phenanthridine core. The synthesis of a range of substituted benzylamine building blocks and their incorporation into the library is
Regioselective copper-catalyzed amination of bromobenzoic acids using aliphatic and aromatic amines.
The Journal of organic chemistry, 71(8), 3270-3273 (2006-04-08)
A chemo- and regioselective copper-catalyzed cross-coupling procedure for amination of 2-bromobenzoic acids is described. The method eliminates the need for acid protection and produces N-aryl and N-alkyl anthranilic acid derivatives in up to 99% yield. N-(1-Pyrene)anthranilic acid has been employed
Developmental cell, 54(6), 742-757 (2020-08-07)
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