Basic Information |
|
| Product Name： | 5-INDOLYLBORONIC ACID |
| CAS： | 144104-59-6 ;17153-20-7 |
| English Synonyms： | 5-INDOLBORONIC ACID ; 5-INDOLYLBORONIC ACID 97% ; BORONIC ACID, B-1H-INDOL-5-YL- ; 5-INDOLE-BORONIC ACID ; 1H-INDOLE-5-BORONIC ACID ; 1H-INDOL-5-YL-5-BORONIC ACID ; INDOLE-5-BORONIC ACID ; 5-BORONO-1H-INDOLE ; 3-METHYLISOXAZOLE-4-CARBOXYLIC ACID, 98+% ; 1H-INDOL-5-YLBORONIC ACID ; 1H-INDOL-5-YLBORANEDIOL ; B-1H-INDOL-5-YL-BORONIC ACID ; 5-INDOLYLBORONIC ACID ; 5-BORONOINDOLE ; 5-INDOLYLBORONIC ACID 95% ; 3-METHYL-4-ISOXAZOLECARBOXYLIC ACID |
| MDL Number.： | MFCD01319013 |
| H bond acceptor： | 3 |
| H bond donor： | 3 |
| Smile： | B(c1ccc2c(c1)cc[nH]2)(O)O |
| InChi： | InChI=1S/C8H8BNO2/c11-9(12)7-1-2-8-6(5-7)3-4-10-8/h1-5,10-12H |
| InChiKey： | InChIKey=VHADYSUJZAPXOW-UHFFFAOYSA-N |
Property |
|
| Melting Point： | 170-175 DEG C/185-187°C |
| Comments： | APPLICATION: REACTANT INVOLVED IN THE SYNTHESIS OF BIOLOGICALLY ACTIVE MOLECULES INCLUDING: INDOLE INHIBITORS OF MMP-13 FOR ARTHRITIC DISEASE TREATMENT. SUBSTITUTED PYRIMIDINES ACTING AS TUBULIN POLYMERIZATION INHIBITORS REACTANT INVOLVED IN SUZUKI COUPLING REACTIONS FOR SYNTHESIS OF ARYL- HETARYLFUROCOUMARINS. ARYL-SUBSTITUTED OXABENZINDOLES AND METHANOBENZINDOLES REACTANT INVOLVED IN: OXIDATIVE CROSS-COUPLING WITH MERCAPTOACETYLENES. TRIFLUOROMETHYLATION APPLICATION: SUBSTRATE USED IN A RHODIUM-CATALYZED 1,4-ADDITION TO UNPROTECTED MALEIMIDES GENERAL DESCRIPTION: MAY CONTAIN VARYING AMOUNTS OF ANHYDRIDE STORAGE TEMPERATURE: 2-8 DEG C UNSPSC: 12352103 WGK: 3 |
Safety information |
|
| Symbol： |
GHS07
|
| 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 |
| WGK Germany： | 3 |
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