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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:
产品名称
3-溴-2-甲基苯胺, 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
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
General description
3-Bromo-2-methylaniline is a 3-halo-2-methylaniline derivative.
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
A practical synthesis of a PI3K inhibitor under noncryogenic conditions via functionalization of a lithium triarylmagnesiate intermediate
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Organic Process Research & Development, 17(1), 97-107 (2013)
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)
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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