3,5-Bis(trifluoromethyl)styrene | CAS:349-59-7
3,5-Bis(trifluoromethyl)styrene
- 名称:3,5-二(三氟甲基)苯乙烯 | 3,5-Bis(trifluoromethyl)styrene
- CAS号:349-59-7
- 别名:1-Ethenyl-3,5-bis(trifluoromethyl)benzene; 3,5-Bis(trifluoromethyl)-1-vinylbenzene
- 分子式:C10H6F6
- 分子量:240.15
- EINESC号:
产品描述
物理化学性质
熔点 | 7-8 ºC** |
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沸点 | 60 ºC (20 Torr)** |
闪点 | 50.0±0.0 ºC, 计算值* |
密度 | 1.316±0.06 g/cm3 (20 º |
折射率 | 1.4220 (25 ºC)** |
安全数据
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SDS
来源 | SDS样本 |
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没有数据 | 没有数据 |
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Synthesis of DNA duplexes containing complexes of 5-modified pyrimidine bases and metal ions.Kenji Iwamoto et al.Nucleic acids symposium series (2004), (51)(51), 181-182 (2007-11-22)
DNA glycosylase activities for thymine residues oxidized in the methyl group are functions of the hNEIL1 and hNTH1 enzymes in human cells.Qiu-Mei Zhang et al.DNA repair, 4(1), 71-79 (2004-11-10)
Mutational analysis of the damage-recognition and catalytic mechanism of human SMUG1 DNA glycosylase.Mayumi Matsubara et al.Nucleic acids research, 32(17), 5291-5302 (2004-10-07)
Identification and characterization of mammalian 5-formyluracil-DNA glycosylase.Mayumi Matsubara et al.Nucleic acids research. Supplement (2001), (3)(3), 233-234 (2003-09-27)
Opposite-base dependent excision of 5-formyluracil from DNA by hSMUG1.Ingeborg Knaevelsrud et al.International journal of radiation biology, 85(5), 413-420 (2009-04-15)
5-Formyluracil-induced perturbations of DNA function.Daniel K Rogstad et al.Biochemistry, 43(19), 5688-5697 (2004-05-12)
Ab initio base-pairing energies of an oxidized thymine product, 5-formyluracil, with standard DNA bases at the BSSE-free DFT and MP2 theory levels.David E Volk et al.Organic & biomolecular chemistry, 5(10), 1554-1558 (2007-06-16)
Qualitative and quantitative analyses of the decomposition products that arise from the exposure of thymine to monochromatic ultrasoft X rays and 60Co gamma rays in the solid state.Ken Akamatsu et al.Radiation research, 161(4), 442-450 (2004-03-25)
An unusual syn conformation of 5-formyluracil stabilized by supramolecular interactions.Gustavo Portalone et al.Acta crystallographica. Section C, Crystal structure communications, 63(Pt 11), o650-o654 (2007-11-09)
Recognition of oxidized thymine base on the single-stranded DNA by replication protein A.Daisuke Irie et al.Nucleosides, nucleotides & nucleic acids, 25(4-6), 439-451 (2006-07-15)
Assessment of DNA Epigenetic Modifications.Bi-Feng Yuan Chemical research in toxicology, 33(3), 695-708 (2019-11-07)
Binding activity of replication protein A to single-stranded DNA containing oxidized pyrimidine base.T Kasama et al.Nucleic acids research. Supplement (2001), (1)(1), 167-168 (2003-07-03)
Ntg1 and Ntg2 proteins as 5-formyluracil-DNA glycosylases/AP lyases in Saccharomyces cerevisiae.Q M Zhang et al.International journal of radiation biology, 79(5), 341-349 (2003-08-29)
A proposed mechanism for the mutagenicity of 5-formyluracil.E J Privat et al.Mutation research, 354(2), 151-156 (1996-07-22)
Identification of 5-formyluracil DNA glycosylase activity of human hNTH1 protein.Izumi Miyabe et al.Nucleic acids research, 30(15), 3443-3448 (2002-07-26)
Thymine hydroperoxide as a potential source of singlet molecular oxygen in DNA.Fernanda M Prado et al.Free radical biology & medicine, 47(4), 401-409 (2009-05-12)
Stable, specific, and reversible base pairing via Schiff base.Chikara Dohno et al.Journal of the American Chemical Society, 127(47), 16681-16684 (2005-11-25)
Cu(II) complexes with heterocyclic substituted thiosemicarbazones: the case of 5-formyluracil. Synthesis, characterization, x-ray structures, DNA interaction studies, and biological activity.Monica Baldini et al.Inorganic chemistry, 42(6), 2049-2055 (2003-03-18)
Ultrasensitive determination of DNA oxidation products by gas chromatography-tandem mass spectrometry and the role of antioxidants in the prevention of oxidative damage.Sam Dawbaa et al.Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 1051, 84-91 (2017-03-24)
Induction of T --> G and T --> A transversions by 5-formyluracil in mammalian cells.Hiroyuki Kamiya et al.Mutation research, 513(1-2), 213-222 (2001-11-24)
Cellular effects of 5-formyluracil in DNA.S Bjelland et al.Mutation research, 486(2), 147-154 (2001-06-27)
Schiff base-mediated base pairing.Chikara Dohno et al.Nucleic acids symposium series (2004), (49)(49), 185-186 (2006-12-08)
Repair of the mutagenic DNA oxidation product, 5-formyluracil.Pingfang Liu et al.DNA repair, 2(2), 199-210 (2003-01-18)
Mutagenicity of 5-formyluracil in mammalian cells.H Kamiya et al.Nucleic acids symposium series, (44)(44), 81-82 (2003-08-09)
Fragmentation of deprotonated ions of oligodeoxynucleotides carrying a 5-formyluracil or 2-aminoimidazolone.Yinsheng Wang et al.Journal of the American Society for Mass Spectrometry, 13(10), 1190-1194 (2002-10-22)
Nucleotide excision repair of 5-formyluracil in vitro is enhanced by the presence of mismatched bases.Katsuhito Kino et al.Biochemistry, 43(10), 2682-2687 (2004-03-10)
Oxidatively Generated Lesions as Internal Photosensitizers for Pyrimidine Dimerization in DNA.Isabel Aparici-Espert et al.ACS chemical biology, 13(3), 542-547 (2018-01-05)
Role of the Escherichia coli and human DNA glycosylases that remove 5-formyluracil from DNA in the prevention of mutations.Q M Zhang Journal of radiation research, 42(1), 11-19 (2001-06-08)
Mammalian 5-formyluracil-DNA glycosylase. 2. Role of SMUG1 uracil-DNA glycosylase in repair of 5-formyluracil and other oxidized and deaminated base lesions.Aya Masaoka et al.Biochemistry, 42(17), 5003-5012 (2003-04-30)
Structural and functional properties of CiNTH, an endonuclease III homologue of the ascidian Ciona intestinalis: critical role of N-terminal region.Seiji Kato et al.Genes & genetic systems, 87(2), 115-124 (2012-07-24)
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