530018
3-溴-2-甲基苯胺
97%
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关于此项目
线性分子式:
Br(CH3)C6H3NH2
化学文摘社编号:
分子量:
186.05
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
259-568-5
MDL number:
Assay:
97%
InChI key
IILVSKMKMOJHMA-UHFFFAOYSA-N
InChI
1S/C7H8BrN/c1-5-6(8)3-2-4-7(5)9/h2-4H,9H2,1H3
SMILES string
Cc1c(N)cccc1Br
assay
97%
refractive index
n20/D 1.619 (lit.)
bp
248 °C (lit.)
density
1.51 g/mL at 25 °C (lit.)
functional group
bromo
General description
3-Bromo-2-methylaniline is a 3-halo-2-methylaniline derivative.
Application
3-Bromo-2-methylaniline may be used in the preparation of :
- 3,4-dibromo-2-methylaniline
- racemic 3,9-dibromo-4,10-dimethyl-6H,12H,5,11-methanodibenzodiazocine, a racemic derivative of Tröger′s base
- 4-bromo-1H-indazole
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
230.0 °F - closed cup
flash_point_c
110 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
此项目有
Synthesis, Resolution, and Absolute Configuration of Difunctionalized Troger's Base Derivatives.
Kiehne U, et al.
Chemistry (Weinheim An Der Bergstrasse, Germany), 14(14), 4246-4255 (2008)
A practical synthesis of a PI3K inhibitor under noncryogenic conditions via functionalization of a lithium triarylmagnesiate intermediate
Tian Q, et al.
Organic Process Research & Development, 17(1), 97-107 (2013)
Efficient and Complementary Methods Offering Access to Synthetically Valuable 1, 2-Dibromobenzenes.
Diemer V, et al.
European Journal of Organic Chemistry, 2011(2), 327-340 (2011)
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