691321
2-溴丙烯醛
95%
别名:
2-Bromo-acrylaldehyde, 2-Bromopropenal
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关于此项目
经验公式（希尔记法）:
C3H3BrO
化学文摘社编号:
分子量:
134.96
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
1698247
InChI
1S/C3H3BrO/c1-3(4)2-5/h2H,1H2
SMILES string
BrC(=C)C=O
InChI key
MDSPECLCFVWIGQ-UHFFFAOYSA-N
assay
94.0-106.0% (AT), 95%
contains
~0.2% hydroquinone as stabilizer
storage temp.
−20°C
Packaging
Bottomless glass bottle. Contents are inside inserted fused cone.
signalword
Danger
Hazard Classifications
Acute Tox. 2 Oral - Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Aquatic Acute 1 - Eye Dam. 1 - Skin Corr. 1B
存储类别
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
wgk
WGK 3
flash_point_f
207.0 °F
flash_point_c
97.2 °C
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
A Chenna et al.
Carcinogenesis, 13(12), 2361-2365 (1992-12-01)
Thymidine was permitted to react with the known mutagens acrolein and 2-bromoacrolein under physiological conditions. The products of these reactions were separated by HPLC and characterized by UV, FAB/MS, electrospray MS, 1H NMR and chemical transformation. The reaction with acrolein
Ming Wah Wong
The Journal of organic chemistry, 70(14), 5487-5493 (2005-07-02)
[structures: see text] Ab initio and density functional calculations were employed to examine the structures and binding energies of various complexes between 2-bromolacrolein and N-tosyl-(S)-tryptophan-derived B-butyl-1,3,2-oxazaborolidin-5-one (NTOB), a catalyst commonly used for Diels-Alder reactions. Our calculations show that the chiral
E Eder et al.
Archives of toxicology, 68(8), 471-479 (1994-01-01)
The reaction of the mutagenic 2-haloacroleins, 2-fluoroacrolein, -2-chloroacrolein and 2-bromoacrolein, with nucleosides and 5'-mononucleotides was studied. We found two different regioisomers of 1,N2-cyclic deoxyguanosine adducts of 2-chloroacrolein and 2-bromoacrolein: type A, the 6-hydroxy, 7-haloadduct in which the OH-substituent is vicinal
G J van Beerendonk et al.
Cancer research, 54(3), 679-684 (1994-02-01)
Calf thymus single-stranded DNA was modified with 2-bromoacrolein (2BA), a genotoxic metabolite of tris(2,3-dibromopropyl)phosphate. This DNA was used as a template for in vitro DNA replication by T7-polymerase and Klenow fragment of Escherichia coli DNA polymerase I. Increasing levels of
S D Nelson et al.
Biochemical and biophysical research communications, 121(1), 213-219 (1984-05-31)
The potent mutagen 2- bromoacrolein is formed from the carcinogenic flame retardant tris(2,3-dibromopropyl)phosphate (Tris-BP) on incubation with hepatic microsomes. Substitution of deuterium for hydrogen at the terminal carbon atoms (C-3) of Tris-BP significantly decreased both the mutagenic response and the
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