Name: | 7-HYDROXY-5-METHYL-1,3,4-TRIAZAINDOLIZINE |
CAS: | 2503-56-2 ;112801-35-1 |
Synonyms: | 7-HYDROXY-5-METHYL-1,3,4-TRIAZAINDOLIZINE ; 6-METHYL-4-HYDROXY-1,3,3A,7-TETRAAZAINDENE ; 5-METHYL-1,3,4-TRIAZAINDOLIZIN-7-OL ; 7-HYDROXY-5-METHYL-[1,2,4]TRIAZOLO[2,3-A]PYRIMIDINE ; 7-HYDROXY-5-METHYL[1,2,4]TRIAZOLO[1,5-A]PYRIMIDINE ; 5 METHYL-5-TRIAZOLO[1,5-A]PYRIMIDIN-7-OL ; 5-METHYL-SYM-TRIAZOLO [1,5-A]PYRIMIDIN-7-OL ; 5-METHYL[1,2,4]TRIAZOLO[1,5-A]PYRIMIDIN-7-OL ; 7-HYDROXY-5-METHYL-1,2,4-TRIAZAINDOLIZINE ; BUTTPARK 125\40-15 ; 5-METHYL-S-TRIAZOLO[1,5-A]PYRIMIDIN-7-OL ; 5-METHYL-7-HYDROXY-1,3,4-TRIAZAINDOLIZINE ; TM 2 ; 5-METHYL-S-TRIAZOLO[1,5-A]PYRIMIDINE-7-OL ; [1,2,4]TRIAZOLO[1,5-A]PYRIMIDIN-7-OL, 5-METHYL- |
MDL.: | MFCD00005555 |
H bond acceptor: | 5 |
H bond donor: | 1 |
Smile: | Cc1cc(n2c(n1)ncn2)O |
InChi: | InChI=1S/C6H6N4O/c1-4-2-5(11)10-6(9-4)7-3-8-10/h2-3,11H,1H3 |
InChiKey: | InChIKey=ZUIVNYGZFPOXFW-UHFFFAOYSA-N |
Property |
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Melting Point: | 280-283 DEG C(LIT) |
Comments: | APPLICATION: REACTANT FOR THE SYNTHESIS OF: RUTHENIUM(II)-HMTPO COMPLEXES. DIHYDROOROTATE DEHYDROGENASE INHIBITORS WITH ANTIMALARIAL ACTIVITY. REACTANT FOR THE VILSMEIER REACTION OF CONJUGATED CARBOCYCLES AND HETEROCYCLES. INVESTIGATIONS OF THE PHARMACOLOGICAL ACTIVITY CAUSED BY BINDING TO HIV TAR RNA. ADDITIVE TO STUDY THE SPACE CHARGE LAYER IN SILVER BROMIDE MICROCRYSTALS NSC 32071 NSC 511493 RTECS: XZ6133300 UNSPSC: 12352100 WGK: 1 |
Safety information |
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Symbol: |
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Signal word: | Warning |
Hazard statements: | H315-H319-H335 |
Precautionary statements: | P261-P305 + P351 + P338 |
hazard symbol: | Xi |
Risk Code: | R:36/37/38 |
Safe Code: | S:26-36 |
WGK Germany: | 1 |
7-HYDROXY-5-METHYL-1,3,4-TRIAZAINDOLIZINE
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