BTB1 - ≥98% , CAS No.86030-08-2

CAS: 86030-08-2 Cat. No.: B288114 Summenformel: C12H8ClNO4S Molekulargewicht: 297.71 EG-Nummer: 692-409-1
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QUALITÄT & REINHEIT ≥98%
Synonyms
4-Chloro-2-nitro-1-(phenylsulfonyl)benzene
Storage
Store at 2-8°C
Shipped In
Wet ice
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Menge
10mg
B288114-10mg
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50mg
B288114-50mg
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249,82€
100mg
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396,47€
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Warum diese Qualität

≥98% für empfindliche chromatographische und analytische Workflows, die minimale Basislinieninterferenzen erfordern.

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Lagerung & Versand

Store at 2-8°C Versand Wet ice. Genaue Spezifikationen finden Sie im chargenspezifischen COA.

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Qualitätsdokumente

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Literaturbeleg

In 0 peer-reviewten Publikationen zu Chromatographie, organischer Synthese und Kreuzkupplungsreaktionen zitiert.

Übersicht

BTB-1 is a potent, selective and reversible mitotic motor protein Kif18A inhibitor with an IC50 of 1.69 μM.


Spezifikationen

Synonyme
4-Chloro-2-nitro-1-(phenylsulfonyl)benzene
Spezifikationen & Reinheit
≥98%
Biochemische und physiologische Mechanismen
Selective and ATP-competitive mitotic kinesin Kif18A inhibitor (IC50= 1.7μM); reversibly inhibits microtubule-stimulated Kif18A ATPase activity. Displays selectivity against a panel of other mitotic kinesins.
Storage
Store at 2-8°C
Verschickt in
Wet ice
Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.
Reinheit
≥98%
Namen und Kennungen
Pubchem Sid
Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/488189317
Kanonisches Lächeln
C1=CC=C(C=C1)S(=O)(=O)C2=C(C=C(C=C2)Cl)[N+](=O)[O-]
IUPAC Name
1-(benzenesulfonyl)-4-chloro-2-nitrobenzene
InChIKey
VZDUQPHKUBZMLW-UHFFFAOYSA-N
INCHI
1S/C12H8ClNO4S/c13-9-6-7-12(11(8-9)14(15)16)19(17,18)10-4-2-1-3-5-10/h1-8H
Isomere SMILES
C1=CC=C(C=C1)S(=O)(=O)C2=C(C=C(C=C2)Cl)[N+](=O)[O-]
Molekulargewicht
297.71
Reaxy-Rn
2538011
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2538011&ln=

Dokumentation

📋 Sicherheitsdatenblatt (SDS)

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✅ Analysezertifikat (COA)

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Erweiterte Daten

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassBenzenoids
KlasseBenzene and substituted derivatives
SubclassNitrobenzenes
Intermediate Tree Nodes Not available
Direct ParentNitrobenzenes
Alternative Parents Benzenesulfonyl compounds  Nitroaromatic compounds  Chlorobenzenes  Aryl chlorides  Sulfones  Propargyl-type 1,3-dipolar organic compounds  Organic oxoazanium compounds  Organopnictogen compounds  Organonitrogen compounds  Organochlorides  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAromatic homomonocyclic compounds
Substituents Benzenesulfonyl group - Nitrobenzene - Nitroaromatic compound - Chlorobenzene - Halobenzene - Aryl chloride - Aryl halide - Sulfone - Sulfonyl - C-nitro compound - Organic nitro compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Organic oxoazanium - Organic 1,3-dipolar compound - Organic nitrogen compound - Organosulfur compound - Organonitrogen compound - Organochloride - Organohalogen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Aromatic homomonocyclic compound
BeschreibungThis compound belongs to the class of organic compounds known as nitrobenzenes. These are compounds containing a nitrobenzene moiety, which consists of a benzene ring with a carbon bearing a nitro group.
External Descriptors Not available
3D-Struktur
Interaktives chemisches Strukturmodell





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Hdac6 Histone deacetylase 6 (222 Activities)
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Wirkungsmechanismen
Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

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8 results found

Lot NumberCertificate TypeDatumArtikel
C2322267C2322267Certificate of AnalysisJan 19, 2026 B288114
C2322271C2322271Certificate of AnalysisJan 19, 2026 B288114
C2322277C2322277Certificate of AnalysisJan 19, 2026 B288114
C2322278C2322278Certificate of AnalysisJan 19, 2026 B288114
C2322282C2322282Certificate of AnalysisJan 19, 2026 B288114
C2322286C2322286Certificate of AnalysisJan 19, 2026 B288114
C2322295C2322295Certificate of AnalysisJan 19, 2026 B288114
C2322296C2322296Certificate of AnalysisJan 19, 2026 B288114
Chemische und physikalische Eigenschaften
LöslichkeitSolvent:DMSO, Max Conc. mg/mL: 29.77, Max Conc. mM: 100; Solvent:ethanol, Max Conc. mg/mL: 5.95, Max Conc. mM: 20
Molekulargewicht297.710 g/mol
XLogP33.300
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count4
Rotatable Bond Count2
Exact Mass296.986 Da
Monoisotopic Mass296.986 Da
Topological Polar Surface Area88.300 Ų
Heavy Atom Count19
Formal Charge0
Complexity422.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Lösungsrechner
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