M29304
N-甲基苯胺
98%
别名:
一甲基苯胺
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关于此项目
线性分子式:
C6H5NHCH3
化学文摘社编号:
分子量:
107.15
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
202-870-9
Beilstein/REAXYS Number:
741982
MDL number:
Assay:
98%
Form:
liquid
产品名称
N-甲基苯胺, 98%
InChI key
AFBPFSWMIHJQDM-UHFFFAOYSA-N
InChI
1S/C7H9N/c1-8-7-5-3-2-4-6-7/h2-6,8H,1H3
SMILES string
CNc1ccccc1
assay
98%
form
liquid
refractive index
n20/D 1.571 (lit.)
bp
196 °C (lit.)
mp
−57 °C (lit.)
density
0.989 g/mL at 25 °C (lit.)
Quality Level
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Application
N-甲基苯胺是用于以下方面的通用试剂：
- 针对铑催化不对称硼氢化制备亚磷酰胺配体。
- 作为C3选择性吲哚甲酰化的甲酰化试剂。
- 合成了一种基于红质的荧光探针，HKGreen-3，用于检测过亚硝酸根。
- 作为合成AKT（蛋白激酶B）抑制剂-IV的关键起始物料。
signalword
Danger
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Irrit. 2 - STOT RE 2 Oral
target_organs
Liver,spleen,Bone marrow
存储类别
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 3
flash_point_f
185.0 °F - closed cup
flash_point_c
85 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
危险化学品
此项目有
Efficient amide-directed catalytic asymmetric hydroboration.
Smith S M, et al.
Journal of the American Chemical Society, 130(12), 3734-3735 (2008)
Synthesis and biological evaluation of analogues of AKT (protein kinase B) inhibitor-IV.
Sun Q, et al.
Journal of Medicinal Chemistry, 54(5), 1126-1139 (2011)
HKGreen-3: a rhodol-based fluorescent probe for peroxynitrite.
Peng T and Yang D
Organic Letters, 12(21), 4932-4935 (2010)
V Arjunan et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 72(2), 436-444 (2008-12-17)
The Fourier transform infrared (FTIR) and FT-Raman spectra of 2-chloro-4-methylaniline and 2-chloro-6-methylaniline have been measured in the range 4000-400 and 4000-100cm(-1), respectively. Utilising the observed FTIR and FT-Raman data, a complete vibrational assignment and analysis of the fundamental modes of
Israel González et al.
Organic letters, 11(8), 1677-1680 (2009-04-10)
N-Methylanilines are readily synthesized in high yields through the copper(II)-promoted coupling of anilines and methylboronic acid. This method represents a new approach for the selective monomethylation of anilines, and it is the first reported example of a Chan-Lam coupling involving
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