Help
RSS
API
Feed
Maltego
Contact
Domain > organoborons.com
×
More information on this domain is in
AlienVault OTX
Is this malicious?
Yes
No
Whois
Property
Value
Email
combichem@gmail.com
NameServer
NS2.ROBOHOST.MOBI
Created
2012-01-21 00:00:00
Changed
2016-01-11 00:00:00
Expires
2017-01-21 00:00:00
Registrar
PDR LTD. D/B/A PUBLI
DNS Resolutions
Date
IP Address
2025-01-17
80.89.228.44
(
ClassC
)
Port 80
HTTP/1.1 301 Moved PermanentlyServer: nginx/1.18.0Date: Mon, 25 Dec 2023 08:39:39 GMTContent-Type: text/html; charsetiso-8859-1Transfer-Encoding: chunkedConnection: keep-aliveLocation: https://organob !DOCTYPE HTML PUBLIC -//IETF//DTD HTML 2.0//EN>html>head>title>301 Moved Permanently/title>/head>body>h1>Moved Permanently/h1>p>The document has moved a hrefhttps://organoborons.com/>here/a>./p>hr>address>Apache/2.4.53 (Debian) Server at organoborons.com Port 80/address>/body>/html>
Port 443
HTTP/1.1 200 OKServer: nginx/1.18.0Date: Mon, 25 Dec 2023 08:39:40 GMTContent-Type: text/html;;charsetUTF-8Content-Length: 6803Connection: keep-aliveAccept-Ranges: noneStatus: 200 OKVary: Accept-Encod !DOCTYPE html PUBLIC -//W3C//DTD HTML 4.01 Transitional//EN http://www.w3.org/TR/html4/loose.dtd>html>head> title>Organoboron compounds | The chemical database/title> meta namedescription contentA freely accessible database of organoboron molecules. Synthesis and propierties (boiling/melting point, refractive indexe, density).> link relstylesheet href/style.css typetext/css>meta http-equivContent-Type contenttext/html; charsetUTF-8>meta nameviewport contentwidthdevice-width, initial-scale1>/head> body>div idspacer_div> table cellspacing0 cellpadding0 idmain_tb aligncenter> tr> td idhead>/td> /tr>tr> td idhead_menu> table width100% cellspacing0 cellpadding0>tr> td> |a href/>Home/a>|a href/boronic-acids/page-1.html>Boronic acids/a>|a href/boronate-esters/page-1.html>Boronate Esters/a>|a href/potassium-trifluoroborates/page-1.html>Trifluoroborates/a>| /td>td idsearch> form action/text-search/search.php methodGET>input typehidden valuesearchform namemode>input typehidden namefield valuenomenclature>table border0 cellpadding2 cellspacing1 classfind>tr>td> input typetext size28 maxlength130 namesearchtext value>/td>td> input typesubmit valueSearch idsearch_but>/td>/tr>/table>/form> /td> /tr>/table> /td> /tr>tr> td idcontent> div classcontent> !-- p classbig>Welcome to Chemical Synthesis Database/p> -->H1>Welcome to Organoboron Compounds Database/H1> p>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./p>p>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 s
View on OTX
|
View on ThreatMiner
Please enable JavaScript to view the
comments powered by Disqus.
Data with thanks to
AlienVault OTX
,
VirusTotal
,
Malwr
and
others
. [
Sitemap
]