Basic Information |
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Product Name: | 1-(TERT-BUTOXYCARBONYL)INDOLE-2-BORONIC ACID |
CAS: | 22396-40-3 ;213318-44-6 |
English Synonyms: | 1H-INDOLE-1-CARBOXYLIC ACID, 2-BORONO-, 1-(1,1-DIMETHYLETHYL) ESTER ; N-(TERT-BUTOXYCARBONYL)-2-INDOLEBORONIC ACID ; INDOLE-2-BORONIC ACID, N-BOC PROTECTED ; N-BOC-INDOL-2-YL BORONIC ACID ; [N-(TERT-BUTOXYCARBONYL)INDOL-2-YL]BORONIC ACID ; 1-T-BUTOXYCARBONYLINDOLE-2-BORONIC ACID ; N-BOC-1-INDOLEBORONIC ACID ; N-BOC-2-INDOLE BORONIC ACID ; 1-(TERT-BUTOXYCARBONYL)-1H-INDOL-2-YL-2-BORONIC ACID ; 1-(TERT-BUTOXYCARBONYL)INDOL-2-YLBORONIC ACID ; 2-BORONIC ACID-1-CARBOXYLIC ACID TERTBUTYL ESTER-INDOLE ; N-BOC-INDOLE-2-BORONIC ACID ; 1-(TERT-BUTOXYCARBONYL)-1H-INDOLE-2-BORONIC ACID ; 1-(TERT-BUTOXYCARBONYL)-1H-INDOL-2-YLBORONIC ACID ; 1-TERT-BUTYLOXYCARBONYL-INDOL-2-BORONIC ACID ; 1H-INDOLE-2-BORONIC ACID, N-BOC PROTECTED ; N-(TERT-BUTOXYCARBONYL)-1H-INDOLE-2-BORONIC ACID ; 1-N-BOC-INDOLE-2-BORONIC ACID ; 1-BOC-2-INDOLEBORONIC ACID ; BESTIPHARMA 114-625 ; 1H-INDOLE-1-CARBOXYLIC ACID, 2-BORONO-, 1,1-DIMETHYLETHYL ESTER ; 1-BOC-1H-INDOLE-2-BORONIC ACID ; 1-(TERT-BUTOXYCARBONYL)INDOLE-2-BORONIC ACID ; 1-BOC-INDOLE-2-BORONIC ACID ; N-(TERT-BUTOXYCARBONYL)INDOLE-2-BORONIC ACID |
MDL Number.: | MFCD02093045 |
H bond acceptor: | 5 |
H bond donor: | 2 |
Smile: | B(c1cc2ccccc2n1C(=O)OC(C)(C)C)(O)O |
InChi: | InChI=1S/C13H16BNO4/c1-13(2,3)19-12(16)15-10-7-5-4-6-9(10)8-11(15)14(17)18/h4-8,17-18H,1-3H3 |
InChiKey: | InChIKey=SVIBPSNFXYUOFT-UHFFFAOYSA-N |
Property |
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Melting Point: | 85-90 DEG C(LIT) |
Comments: | APPLICATION: REACTANT INVOLVED IN: SUZUKI-MIYAURA CROSS-COUPLING REACTIONS. COPPER-CATALYZED TRIFLUOROMETHYLATION. PALLADIUM-CATALYZED BENZYLATION. HOMOCOUPLING REACTIONS APPLICATION: USED IN A SYNTHESIS OF HYDROXYQUINONES VIA SUZUKI-MIYAURA COUPLING OF PHENYLIDONIUM YLIDES OF HYDROXYQUINONES GENERAL DESCRIPTION: MAY CONTAIN VARYING AMOUNTS OF ANHYDRIDE STORAGE TEMPERATURE: -20 DEG C UNSPSC: 12352103 WGK: 3 |
Safety information |
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WGK Germany: | 3 |
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