CAS 873-83-6
:6-Aminouracile
- 2,4(1H,3H)-Pyrimidinedione, 6-amino-
- 2,4-Dihydroxy-6-aminopyrimidine
- 4-Amino uracil
- 4-Aminouracil
- 6-Amino-2,4(1H,3H)-pyrimidinedione
- 6-Amino-2,4-dihydroxypyrimidine
- 6-Amino-2,4-dioxo-1,2,3,4-tetrahydropyrimidine
- 6-Amino-2,4-pyrimidinediol
- 6-Aminopyrimidine-2,4(1H,3H)-dione
- 6-Aminopyrimidine-2,4-Diol
- 6-Aminouracil
- Aminouracil
- NSC 15919
- NSC 7367
- Voir plus de synonymes
6-Aminouracil, 98%
CAS :This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Sci
Formule :C4H5N3O2Degré de pureté :98%Couleur et forme :White to yellow or cream to pale brown, PowderMasse moléculaire :127.106-Aminouracil
CAS :Formule :C4H5N3O2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :127.10146-Aminouracil
CAS :Formule :C4H5N3O2Degré de pureté :>98.0%(T)(HPLC)Couleur et forme :White to Yellow powder to crystalMasse moléculaire :127.106-Aminouracil
CAS :6-AminouracilFormule :C4H5N3O2Degré de pureté :98%Couleur et forme : yellow solidMasse moléculaire :127.10139g/mol4-Amino-2,6-dihyroxypyrimidine
CAS :Formule :C4H5N3O2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :127.1036-Amino-2,4-dihydroxypyrimidine
CAS :Produit contrôléApplications 6-Amino-2,4-dihydroxypyrimidine (cas# 873-83-6) is a compound useful in organic synthesis.
References Ghahremanzadeh, R., et al.: Chem. Pharm. Bull., 56, 1617 (2008), Bharate, S., et al.: Bioorg. Med. Chem., 16, 7167 (2008), Reigan, P., et al.: Eur. J. Med. Chem., 43, 1248 (2008),Formule :C4H5N3O2Couleur et forme :NeatMasse moléculaire :127.16-Aminouracil
CAS :6-Aminouracil is a hydroxylated form of uracil. It has inhibitory properties against protein synthesis in bacteria, acting as an inhibitor of the enzyme dihydroorotase. 6-Aminouracil has been shown to be effective against PC3 cells and has high resistance to hydrolysis by acid or alkali. The reaction mechanism for the conversion of uracil to 6-aminouracil is unclear; however, it may involve a nucleophilic attack on the hydroxyl group.
Formule :C4H5N3O2Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :127.1 g/molRef: 3D-FA11068
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