448958
Thymine-1-acetic acid
98%
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About This Item
Empirical Formula (Hill Notation):
C7H8N2O4
CAS Number:
Molecular Weight:
184.15
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Product Name
Thymine-1-acetic acid, 98%
Quality Level
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)
SMILES string
CC1=CN(CC(O)=O)C(=O)NC1=O
InChI key
TZDMCKHDYUDRMB-UHFFFAOYSA-N
assay
98%
form
solid
mp
272-278 °C (dec.) (lit.)
functional group
carboxylic acid
Related Categories
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Nan Wang et al.
Biosensors & bioelectronics, 79, 320-326 (2016-01-01)
A sensitive, selective and reusable electrochemical biosensor for the determination of mercury ions (Hg(2+)) has been developed based on thymine (T) modified gold nanoparticles/reduced graphene oxide (AuNPs/rGO) nanocomposites. Graphene oxide (GO) was electrochemically reduced on a glassy carbon substrate. Subsequently
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 =
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)
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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