추천 제품
vapor pressure
0.05 mmHg ( 20 °C)
분석
≥98%
형태
powder
mp
116-118 °C (lit.)
SMILES string
NC(=O)CCl
InChI
1S/C2H4ClNO/c3-1-2(4)5/h1H2,(H2,4,5)
InChI key
VXIVSQZSERGHQP-UHFFFAOYSA-N
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애플리케이션
2-Chloroacetamidecan be used as a reactant to synthesize:
- 2-Amino-4-chloroquinolines via o-alkylation of 4-chloro-1H-quinolin-2-ones and subsequent Smiles rearrangement.
- 2-(Formylaryloxy)acetamides by reacting with hydroxybenzaldehydes in the presence of potassium carbonate as a base.
- Biarylamine derivatives via aluminum triflate-catalyzed direct amination of benzhydrols.
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 3 Oral - Repr. 2 - Skin Sens. 1
Storage Class Code
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
WGK
WGK 2
Flash Point (°F)
338.0 °F
Flash Point (°C)
170 °C
개인 보호 장비
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
이미 열람한 고객
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Solid-phase microextraction coupled with gas chromatography-mass spectrometry (SPME-GC-MS) was used to analyze two triazine (atrazine and simazine) and three chloroacetamide herbicides (acetochlor, alachlor, and metolachlor) in water samples from a midwest US agricultural drainage ditch for two growing seasons. The
Journal of agricultural and food chemistry, 59(9), 4614-4621 (2011-03-23)
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Nature cell biology, 21(4), 442-451 (2019-03-20)
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Environmental science & technology, 39(17), 6561-6574 (2005-09-30)
Although laboratory studies have revealed that many different neutral degradates of chloroacetamide herbicides can form during thermochemical, biological, and photochemical transformations, relatively few have been sought in the environment, despite their likely generation in appreciable amounts, relative persistence, and known
문서
In this study, we developed a rapid trypsin digest kit that, at elevated temperatures, yielded reliable, reproducible results in less than 2 hours on a wide variety of substrates for mass spectrometry.
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