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线性分子式:
BrC6H3(F)CHO
化学文摘社编号:
分子量:
203.01
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
298-056-6
MDL number:
产品名称
5-溴-2-氟苯甲醛, 97%
InChI key
MMFGGDVQLQQQRX-UHFFFAOYSA-N
InChI
1S/C7H4BrFO/c8-6-1-2-7(9)5(3-6)4-10/h1-4H
SMILES string
Fc1ccc(Br)cc1C=O
assay
97%
refractive index
n20/D 1.57 (lit.)
bp
230 °C (lit.)
density
1.71 g/mL at 25 °C (lit.)
functional group
aldehyde
bromo
fluoro
storage temp.
2-8°C
Quality Level
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
10 - Combustible liquids
wgk
WGK 3
flash_point_f
228.9 °F - closed cup
flash_point_c
109.4 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
新产品
此项目有
Synthesis of 5-cyanoindazole and 1-methyl and 1-aryl-5-cyanoindazoles.
Halley F and Sava X.
Synthetic Communications, 27(7), 1199-1207 (1997)
High throughput synthesis of diverse 2, 5-disubstituted indoles using titanium carbenoids bearing boronate functionality.
Main CA, et al.
Tetrahedron, 64(5), 901-914 (2008)
Christian Ruzié et al.
The Journal of organic chemistry, 78(15), 7741-7748 (2013-07-16)
The synthesis of 1,6-, 2,7-, 3,8-, and 4,9-isomers of dibromo- and didodecyl[1]benzothieno[3,2-b][1]benzothiophenes, via the stilbene pathway, is described. Starting from the synthesis of bromo-2-(methylthio)benzaldehydes, a series of functionalization, McMurry coupling, and finalising cyclization reactions were explored. The stereochemistry of the
Keith W Woods et al.
Bioorganic & medicinal chemistry, 14(20), 6832-6846 (2006-07-18)
A series of heteroaryl-pyridine containing inhibitors of Akt are reported. The synthesis and structure-activity relationships are discussed, leading to the discovery of a indazole-pyridine analogue (K(i)=0.16 nM). These compounds bind in the ATP binding site, are potent, ATP competitive, and
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