产品名称
炔丙基溴 溶液, 80 wt. % in xylene
InChI
1S/C3H3Br/c1-2-3-4/h1H,3H2
SMILES string
BrCC#C
InChI key
YORCIIVHUBAYBQ-UHFFFAOYSA-N
concentration
80 wt. % in xylene
refractive index
n20/D 1.494
bp
97 °C
density
1.34 g/mL at 25 °C
functional group
alkyl halide
bromo
storage temp.
2-8°C
Quality Level
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Application
Propargyl bromide solution (80wt.% solution in xylene) may be used in the preparation of dimethyl 5-hydroxyisophthalate propargyl ether.
General description
The product is an 80wt.% solution of propargyl bromide (3-bromo-1-propyne) in xylene.
signalword
Danger
Hazard Classifications
Acute Tox. 3 Oral - Asp. Tox. 1 - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1B - STOT RE 2 Inhalation - STOT SE 3
target_organs
Central nervous system,Liver,Kidney, Respiratory system
存储类别
3 - Flammable liquids
wgk
WGK 2
flash_point_f
45.0 °F - closed cup
flash_point_c
7.22 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
新产品
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Self-assembly of amphiphilic polymeric dendrimers synthesized with selective degradable linkages.
Urbani CN, et al.
Macromolecules, 41(1), 76-86 (2008)
Francesco Alessandrini et al.
International immunopharmacology, 29(1), 105-109 (2015-06-03)
The involvement of muscarinic receptors in cancer has been reported. Recently we have demonstrated that the activation of M2 muscarinic receptors, through arecaidine propargyl ester, arrests cell proliferation and induces apoptosis in primary and established glioblastoma cell lines. Considering the
Maria Di Bari et al.
Neurochemistry international, 90, 261-270 (2015-10-13)
Glioblastomas are the most common brain tumors in humans. Previously, we demonstrated that the muscarinic receptor agonist, arecaidine propargyl ester, via M2 receptors, inhibits cell proliferation in a time and dose-dependent manner and induces a severe apoptosis in human U251
Jong Hwan Kwak et al.
Biomaterials, 61, 52-60 (2015-05-23)
We studied the blood-brain barrier (BBB) permeability and intracellular localization of a fluorescein isothiocyanate (FITC)-labeled dieckol (1) and a rhodamine B-labeled dieckol (7), for exploring the possible therapeutic application of fluorone-labeled dieckols in neurodegenerative diseases. Both compounds (1 &7) were
Abdelaziz Al Ouahabi et al.
Journal of the American Chemical Society, 137(16), 5629-5635 (2015-04-09)
Sequence-defined non-natural polyphosphates were prepared using iterative phosphoramidite protocols on a polystyrene solid support. Three monomers were used in this work: 2-cyanoethyl (3-dimethoxytrityloxy-propyl) diisopropylphosphoramidite (0), 2-cyanoethyl (3-dimethoxytrityloxy-2,2-dimethyl-propyl) diisopropylphosphoramidite (1), and 2-cyanoethyl (3-dimethoxytrityloxy-2,2-dipropargyl-propyl) diisopropylphosphoramidite (1'). Phosphoramidite coupling steps allowed rapid synthesis
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