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Merck
CN

A88204

间茴香胺

97%

别名:

3-氨基苯甲醚, 3-甲氧基苯胺

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线性分子式:
CH3OC6H4NH2
化学文摘社编号:
分子量:
123.15
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
208-651-4
Beilstein/REAXYS Number:
386119
MDL number:
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产品名称

间茴香胺, 97%

InChI

1S/C7H9NO/c1-9-7-4-2-3-6(8)5-7/h2-5H,8H2,1H3

InChI key

NCBZRJODKRCREW-UHFFFAOYSA-N

SMILES string

COc1cccc(N)c1

assay

97%

form

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.)

Quality Level

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Application

m -茴香胺用于:
  • 合成 N -取代-3-氯-2-氮杂环丁烷酮,后者是潜在的驱虫剂。
  • 铑催化合成吲哚 和铜催化合成苯并咪唑。
  • 制备偶氮杯芳烃染料。

signalword

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - STOT RE 2

存储类别

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

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

法规信息

危险化学品
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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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)
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)
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)

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