추천 제품
애플리케이션
4-Chloroaniline can undergo:
- Allylation in the presence of ultrasonication to form N-allyl-4-chloroaniline, a precursor for bioactive compounds containing indole and dihydroindole nucleus.
- Povarov reaction with cyclopentadiene to form C-2 aliphatic substituted tetrahydroquinolines.
- Mannich reaction with aldehydes and cyclic ketones to form β-amino carbonyl compounds.
- Nitration to form 4-chloro-3-nitroaniline in the presence of guanidinium nitrate.
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 1B - Skin Sens. 1
Storage Class Code
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
WGK
WGK 3
Flash Point (°F)
248.0 °F - closed cup
Flash Point (°C)
120.0 °C - closed cup
개인 보호 장비
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
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
Factorial study to assess an ultrasonic methodology for the allylation of 4-chloroaniline
Green Processing and Synthesis, 6(2), 203-209 (2017)
Guanidinium nitrate: a novel reagent for aryl nitrations
Tetrahedron Letters, 45(47), 8681-8683 (2004)
Highly efficient one-pot, three-component Mannich reaction catalysed by boric acid and glycerol in water with major `syn?diastereoselectivity
Tetrahedron Letters, 50(29), 4246-4250 (2009)
Lanthanide (III)-catalyzed multi-component aza-Diels-Alder reaction of aliphatic N-arylaldimines with cyclopentadiene.
Tetrahedron Letters, 44(41), 7569-7573 (2003)
Journal of endodontics, 34(12), 1521-1523 (2008-11-26)
The combination of chlorhexidine and EDTA produces a white precipitate. The aim of this study was to determine if the precipitate involves the chemical degradation of chlorhexidine. The precipitate was produced and redissolved in a known amount of dilute trifluoroacetic
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