448958
胸腺嘧啶-1-乙酸
98%
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关于此项目
经验公式（希尔记法）:
C7H8N2O4
化学文摘社编号:
分子量:
184.15
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
方案
98%
表单
solid
mp
272-278 °C (dec.) (lit.)
官能团
carboxylic acid
SMILES字符串
CC1=CN(CC(O)=O)C(=O)NC1=O
InChI
1S/C7H8N2O4/c1-4-2-9(3-5(10)11)7(13)8-6(4)12/h2H,3H2,1H3,(H,10,11)(H,8,12,13)
InChI key
TZDMCKHDYUDRMB-UHFFFAOYSA-N
警示用语：
Warning
危险声明
危险分类
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
Giant vesicle formation through self-assembly of complementary random copolymers.
Ilhan F, et al.
Journal of the American Chemical Society, 122(24), 5895-5896 (2000)
Pilar Amo-Ochoa et al.
Inorganic chemistry, 52(19), 11428-11437 (2013-09-18)
Four new copper(II) coordination complexes, obtained by reaction of CuX2 (X = acetate or chloride) with thymine-1-acetic acid and uracil-1-propionic acid as ligands, of formulas [Cu(TAcO)2(H2O)4]·4H2O (1), [Cu(TAcO)2(H2O)2]n (2), [Cu3(TAcO)4(H2O)2(OH)2]n·4H2O (3), and [Cu3(UPrO)2Cl2(OH)2(H2O)2]n (4) (TAcOH = thymine-1-acetic acid, UPrOH =
Domenica Musumeci et al.
International journal of nanomedicine, 13, 2613-2629 (2018-05-12)
Nucleobase-bearing peptides and their interaction with DNA and RNA are an important topic in the development of therapeutic approaches. On one hand, they are highly effective for modulating the nucleic-acid-based biological processes. On the other hand, they permit to overcome
Ojodomo J Achadu et al.
Mikrochimica acta, 185(10), 461-461 (2018-09-17)
A microwave-assisted hydrothermal method was employed to prepare thymine-modified graphitic carbon nitride quantum dots (T-gCNQDs) which are shown to be a novel fluorescent nanoprobe for Hg(II). They exhibit excellent optical properties (blue emission with a fluorescence quantum yield of 46%)
P J Finn et al.
Nucleic acids research, 24(17), 3357-3363 (1996-09-01)
Adenine, thymine and cytosine PNA monomers have been prepared using 3-amino-1,2-propanediol as a starting material. The benzoyl group was used to protect the exocyclic amines of the heterocyclic bases of A and C PNA monomers and the backbone primary amine
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