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About This Item
Empirical Formula (Hill Notation):
C7H9N3O2S
CAS Number:
Molecular Weight:
199.23
MDL number:
UNSPSC Code:
41106305
PubChem Substance ID:
NACRES:
NA.51
biological source
synthetic
form
liquid
storage temp.
−20°C
SMILES string
CCSc1ncc(C(O)=O)c(N)n1
InChI
1S/C7H9N3O2S/c1-2-13-7-9-3-4(6(11)12)5(8)10-7/h3H,2H2,1H3,(H,11,12)(H2,8,9,10)
InChI key
TYAKXNHFMATCHA-UHFFFAOYSA-N
Application
4-Amino-5-carboxy-2-ethylmercaptopyrimidine is a derivitized 2-mercaptopyrimidine.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
10 - Combustible liquids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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W Ciesielski et al.
Talanta, 47(3), 745-752 (2008-10-31)
A new method for the determination of 2-mercaptopyrimidines, using their reaction with iodine in neutral and alkaline medium, is presented. The determinability range in the volumetric titration, in phosphate buffer with starch as an indicator, was found to be equal
Chun-Yu Lin et al.
Anticancer research, 22(2A), 937-942 (2002-05-17)
Free radicals and reactive oxygen metabolites have been implicated as important pathologic mediators in many clinical disorders and diseases. An efficient method of detecting the free radical scavenger effect is through xanthine oxidase (XO) inhibition. The inhibition efficiency on XO
Xiu-Hua Zhang et al.
Bioelectrochemistry (Amsterdam, Netherlands), 65(1), 41-46 (2004-11-04)
4-Amino-2-mercaptopyrimidine self-assembled monolayer (AMP SAMs/Au) was prepared on a gold electrode. The AMP SAMs/Au was characterized by using attenuated total reflection-fourier transform infrared (ATR-FTIR) and A.C. Impedance. The electrochemical behavior of brucine on AMP SAMs/Au was studied by cyclic voltammetry
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