추천 제품
Quality Level
분석
97%
양식
liquid
refractive index
n20/D 1.581 (lit.)
bp
251 °C (lit.)
mp
−1-1 °C (lit.)
density
1.096 g/mL at 25 °C (lit.)
SMILES string
COc1cccc(N)c1
InChI
1S/C7H9NO/c1-9-7-4-2-3-6(8)5-7/h2-5H,8H2,1H3
InChI key
NCBZRJODKRCREW-UHFFFAOYSA-N
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관련 카테고리
애플리케이션
m-Anisidine is used in:
- The synthesis of N-substituted-3-chloro-2-azetidinones, which are potential anthelmintic agents.
- Rhodium-catalyzed synthesis of indoles and copper-catalyzed synthesis of benzimidazoles.
- In the preparation of azocalix[4]arene dyes.
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 - STOT RE 2
Storage Class Code
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
WGK
WGK 1
Flash Point (°F)
258.8 °F - closed cup
Flash Point (°C)
126 °C - closed cup
개인 보호 장비
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
가장 최신 버전 중 하나를 선택하세요:
시험 성적서(COA)
Lot/Batch Number
이미 열람한 고객
N-Substituted-3-chloro-2-azetidinones: synthesis and characterization of novel anthelmintic agents.
Kumar M V, et al.
Research Journal of Pharmaceutical, Biological and Chemical Sciences, 1(2), 52-58 (2010)
Yasemin Bektas et al.
Scientific reports, 6, 29554-29554 (2016-07-15)
Synthetic elicitors are drug-like compounds that are structurally distinct from natural defense elicitors. They can protect plants from diseases by activating host immune responses and can serve as tools for the dissection of the plant immune system as well as
Indole synthesis via rhodium catalyzed oxidative coupling of acetanilides and internal alkynes.
Stuart D R, et al.
Journal of the American Chemical Society, 130(49), 16474-16475 (2008)
Azocalixarenes. 1: synthesis, characterization and investigation of the absorption spectra of substituted azocalix [4] arenes.
Karc? F, et al.
Dyes and Pigments, 59(1), 53-61 (2003)
C? H Functionalization/C? N Bond Formation: Copper?Catalyzed Synthesis of Benzimidazoles from Amidines.
Brasche G and Buchwald S L
Angewandte Chemie (International Edition in English), 47(10), 1932-1934 (2008)
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