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Merck
CN

16125

顺-3-溴丙烯酸乙酯

≥99.0% (GC)

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关于此项目

经验公式(希尔记法):
C5H7BrO2
化学文摘社编号:
分子量:
179.01
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
1902817
Assay:
≥99.0% (GC)
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产品名称

顺-3-溴丙烯酸乙酯, ≥99.0% (GC)

InChI

1S/C5H7BrO2/c1-2-8-5(7)3-4-6/h3-4H,2H2,1H3/b4-3-

SMILES string

CCOC(=O)\C=C/Br

InChI key

UJTJVQIYRQALIK-ARJAWSKDSA-N

assay

≥99.0% (GC)

refractive index

n20/D 1.481

density

1.48 g/mL at 20 °C

functional group

bromo
ester

storage temp.

2-8°C

Application

用于立体选择性制备顺式-2-烯醇酯的结构单元

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - 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

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

法规信息

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分析证书(COA)

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Michael B Otteneder et al.
Proceedings of the National Academy of Sciences of the United States of America, 103(17), 6665-6669 (2006-04-15)
3-(2-Deoxy-beta-D-erythro-pentofuranosyl)pyrimido[1,2-alpha]purin-10(3H)-one (M1dG) is a DNA adduct arising from the reaction of 2-deoxyguanosine with the lipid peroxidation product, malondialdehyde, or the DNA peroxidation product, base propenal. M1dG is mutagenic in bacteria and mammalian cells and is present in the genomic DNA
Jozsef Szekely et al.
Nucleosides, nucleotides & nucleic acids, 27(2), 103-109 (2008-01-22)
Short, "one-pot" syntheses of malondialdehyde adducts of deoxyguanosine, deoxyadenosine, and deoxycytidine are described. These syntheses proceed in improved yield and easier purification than previous syntheses and are well suited for the preparation of isotopically labeled nucleoside adducts for biomarker and
A.B. Smith et al.
Tetrahedron Letters, 26, 4419-4419 (1985)
X. Lu et al.
Tetrahedron Letters, 33, 2535-2535 (1992)
Alessio Grimaldi et al.
Communications biology, 3(1), 85-85 (2020-02-27)
Here, we developed an unbiased, functional target-discovery platform to identify immunogenic proteins from primary non-small cell lung cancer (NSCLC) cells that had been induced to apoptosis by cisplatin (CDDP) treatment in vitro, as compared with their live counterparts. Among the

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