4,5-Diamino-6-hydroxy-2-mercapto pyrimidine

CAS: 1004-76-8

Ref. 3D-FD21455

Product Information

• Name: 4,5-Diamino-6-hydroxy-2-mercapto pyrimidine
• Synonyms: 5,6-Diamino-2-thiouracil4,5-Diamino-2-mercaptopyrimidine-6-ol, 2-Mercapto-4,5-diamino-6-hydroxypyrimidine, 2-Mercapto-4-hydroxy-5,6-diamino-pyrimidine, 4(1H)-Pyrimidinone, 5,6-diamino-2,3-dihydro-2-thioxo-, 4,5-Diamino-2-Mercaptopyrimidine-6-Ol, 4,5-Diamino-2-mercaptopyrimidin-6-ol, 4,5-Diamino-6-hydroxy-2-mercaptopyrimidine, 4-5-Diamino-6-Hydroxy-2-*Mercaptopyrimidine Free, 5,6-Diamino-2,3-dihydro-2-thioxo-4(1H)-pyrimidinone, 5,6-Diamino-2-Mercaptopyrimidin-4-Ol, 5,6-Diamino-2-mercapto-1H-pyrimidin-4-one, 5,6-Diamino-2-mercapto-pyrimidin-4-ol, 5,6-Diamino-2-thiouracil, 5,6-Diamino-4-Hydroxy-2-Mercaptopyrimidine, 5,6-diamino-2-thioxo-2,3-dihydropyrimidin-4(1H)-one, NSC 147804, NSC 45759, Uracil, 5,6-diamino-2-thio-

Description

4,5-Diamino-6-hydroxy-2-mercaptopyrimidine is a primary amino that binds to the sulfur in a molecule. It has potent antibacterial activity and can be used for desulfurization of petroleum products. 4,5-Diamino-6-hydroxy-2-mercaptopyrimidine has been shown to react with some cancer cells in vitro and may be used as an anticancer agent. It can also be used as a catalyst for the oxidation of organic compounds in wastewater treatment or hydrochloric acid production. 4,5-Diamino-6-hydroxy-2-mercaptopyrimidine can be synthesized by reacting 3 mercapto propionic acid with 5 aminopyrimidines. The synthesis was optimized using a kinetic method and coordination chemistry. It has also been shown to inhibit cell growth when used on human erythrocytes using patch clamp experiments and assays.br>br

• Brand: Biosynth

Chemical properties

• Molecular weight: 158.18 g/mol
• Formula: C₄H₆N₄OS
• Purity: Min. 95%
• Color/Form: Off-White Powder
• InChI: InChI=1S/C4H6N4OS/c5-1-2(6)7-4(10)8-3(1)9/h5H2,(H4,6,7,8,9,10)
• InChI key: InChIKey=QYSWOQHLIDKEOL-UHFFFAOYSA-N
• SMILES: Nc1[nH]c(=S)[nH]c(=O)c1N