产品名称
3-溴-4-甲基苯甲酸, technical grade, 85%
InChI key
ZFJOMUKPDWNRFI-UHFFFAOYSA-N
InChI
1S/C8H7BrO2/c1-5-2-3-6(8(10)11)4-7(5)9/h2-4H,1H3,(H,10,11)
SMILES string
Cc1ccc(cc1Br)C(O)=O
grade
technical grade
assay
85%
form
solid
mp
200-202 °C (lit.)
200-204 °C
functional group
bromo
carboxylic acid
Application
3-Bromo-4-methylbenzoic acid has been used in the synthesis of:
- biphenyl amides
- 2-benzazepine-4-acetic acid derivative, as an analog of the potent, nonpeptide GPIIb/IIIa antagonist
- O-spiro C-aryl glucosides
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
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
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
法规信息
新产品
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Richard M Angell et al.
Bioorganic & medicinal chemistry letters, 18(1), 324-328 (2007-11-06)
The biphenyl amides are a novel series of p38 MAP kinase inhibitors. Structure-activity relationships of the series against p38alpha are discussed with reference to the X-ray crystal structure of an example. The series was optimised rapidly to a compound showing
Baihua Xu et al.
Bioorganic & medicinal chemistry letters, 19(19), 5632-5635 (2009-08-25)
Two series of O-spiro C-aryl glucosides were synthesized and tested for inhibition of hSGLT1 and hSGLT2. 6'-O-Spiro C-aryl glucosides exhibited potent in vitro hSGLT2 inhibitory activity but 2'-O-spiro C-aryl glucosides showed no in vitro hSGLT2 inhibitory activity at a screening
Wayne Huberty et al.
Journal of fluorescence, 26(2), 609-615 (2016-01-10)
A labeled green fluorescent polystyrene sulfonate (LNaPSS) has been synthesized using atom transfer radical polymerization of a styrene sulfonate monomer with a fluorescent co-monomer, fluorescein thiocyanate-vinyl aniline. As a result this 100 % sulfonated polymer contains no hydrophobic patches along
Synthesis of a 2-benzazepine analog of a potent, nonpeptide GPIIb/IIIa antagonist.
Miller WH, et al.
Tetrahedron Letters, 36(3), 373-376 (1995)
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