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Title | Organoboron compounds | The chemical |
Description | Welcome to Organoboron Compounds A freely accessible database of organoboron molecules. Synthesis and propierties (boiling/melting point, refractive indexe, |
Keywords | N/A |
WebSite | organoborons.com |
Host IP | 185.17.120.27 |
Location | Russian Federation |
Site | Rank |
US$348,713
Last updated: 2023-05-12 06:58:51
organoborons.com has Semrush global rank of 30,352,514. organoborons.com has an estimated worth of US$ 348,713, based on its estimated Ads revenue. organoborons.com receives approximately 40,237 unique visitors each day. Its web server is located in Russian Federation, with IP address 185.17.120.27. According to SiteAdvisor, organoborons.com is safe to visit. |
Purchase/Sale Value | US$348,713 |
Daily Ads Revenue | US$322 |
Monthly Ads Revenue | US$9,657 |
Yearly Ads Revenue | US$115,880 |
Daily Unique Visitors | 2,683 |
Note: All traffic and earnings values are estimates. |
Host | Type | TTL | Data |
organoborons.com. | A | 14399 | IP: 185.17.120.27 |
organoborons.com. | NS | 86400 | NS Record: ns2.robohost.org. |
organoborons.com. | NS | 86400 | NS Record: ns1.robohost.org. |
organoborons.com. | MX | 14400 | MX Record: 0 organoborons.com. |
organoborons.com. | TXT | 14400 | TXT Record: v=spf1 +a +mx +ip4:185.17.120.5 +ip4:64.20.56.10 ~all |
| Home | Boronic acids | Boronate Esters | Trifluoroborates | Welcome to Chemical Synthesis Database --> Welcome to Organoboron Compounds Database Boronic acids and their esters are highly popular synthetic intermediates in organic synthesis for their ease and efficiency of conversion to other functional groups, in metal-catalyzed cross-coupling reactions and for their unique biochemical activity. The palladium-catalyzed cross-coupling reaction of organoboron compounds with organic halides or pseudo-halides - the Suzuki-Miyaura reaction - is a remarkably useful tool in organic synthesis. A new class of air-stable boronic acid derivatives is trifluoroborates, which are offering a unique alternative to most boronic acids, esters and organoboranes for use in Suzuki-Miyaura and other transition-metal-catalyzed cross-coupling reactions. As inhibitors of serine proteases, boronic acids inhibit therapeutically relevant proteases and proteasomes. FDA has approved the first boron-containing |
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