Stattic - Moligand™,≥98% , CAS No.19983-44-9

Name: Stattic - Moligand™,≥98% , CAS No.19983-44-9
Brand: Aladdin Scientific
SKU: S129623
Availability: InStock

CAS: 19983-44-9 Cat. No.: S129623 Molecular Weight: 211.19 EC Number: 633-746-6 PubChem CID: 2779853

COA

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Stattic - Moligand™,≥98% CAS No(19983-44-9) by Aladdin Scientific

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AVAILABLE TO ORDER

GRADE & PURITY Moligand™ ? ≥98%

Synonyms

C8H5NO4S | FT-0621264 | HY-13818 | PB27460 | CCG-222352 | DTXSID70381575 | EC-000.2451 | HMS556B22 | 6-nitro-1lambda6-benzothiophene-1,1-dione | Z595059248 | Maybridge1_005148 | SW219435-1 | CHEBI:86989 | 6-nitro-1 | BCP13194 | HMS3263A18 | Q27159314 | SC

Storage

Store at -20°C

Shipped In

Ice chest + Ice pads

Overview Specifications Names and Identifiers Documentation Advanced Data Taxonomic Classification 3D Structure Associated Targets(Human) Associated Targets(non-human) Mechanisms of Action Certificates（CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Documents & Articles Solution Calculators Reviews

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Why this grade

Moligand™,≥98% Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Store at -20°C Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.

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Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

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Literature proof

Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

Stattic is a potent inhibitor of STAT3, used for cancer treatment.
An inhibitor of Stat3 activation

Specifications

Synonyms

C8H5NO4S | FT-0621264 | HY-13818 | PB27460 | CCG-222352 | DTXSID70381575 | EC-000.2451 | HMS556B22 | 6-nitro-1lambda6-benzothiophene-1, 1-dione | Z595059248 | Maybridge1_005148 | SW219435-1 | CHEBI:86989 | 6-nitro-1 | BCP13194 | HMS3263A18 | Q27159314 | SC

Specifications & Purity

Moligand™, ≥98%

Biochemical and Physiological Mechanisms

Stat3 Inhibitor V, Stattic is a small molecule shown to selectively inhibit the activation of the Stat3 transcription factor by blocking phosphorylation and dimerization events. Stattic has been used as a tool for probing the upstream activation of this f

Storage

Store at -20°C

Shipped In

Ice chest + Ice pads

This product requires cold chain shipping. Ground and other economy services are not available.

Grade

Moligand™

Action Type

INHIBITOR

Note

Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.

Purity

≥98%

Names and Identifiers

Pubchem Sid	504762051
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/504762051
Canonical Smiles	C1=CC(=CC2=C1C=CS2(=O)=O)[N+](=O)[O-]
IUPAC Name	6-nitro-1-benzothiophene 1,1-dioxide
InChIKey	ZRRGOUHITGRLBA-UHFFFAOYSA-N
INCHI	1S/C8H5NO4S/c10-9(11)7-2-1-6-3-4-14(12,13)8(6)5-7/h1-5H
Isomeric SMILES	C1=CC(=CC2=C1C=CS2(=O)=O)[N+](=O)[O-]
WGK Germany	3
PubChem CID	2779853
Molecular Weight	211.19

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organic 1,3-dipolar compounds
  - Class Allyl-type 1,3-dipolar organic compounds
    - Subclass Organic nitro compounds
      - Level5 C-nitro compounds
        Level6 Nitroaromatic compounds

Kingdom	Organic compounds
Superclass	Organic 1,3-dipolar compounds
Class	Allyl-type 1,3-dipolar organic compounds
Subclass	Organic nitro compounds
Intermediate Tree Nodes	C-nitro compounds
Direct Parent	Nitroaromatic compounds
Alternative Parents	Benzenoids Sulfones Propargyl-type 1,3-dipolar organic compounds Organoheterocyclic compounds Organic oxoazanium compounds Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives
Molecular Framework	Aromatic heteropolycyclic compounds
Substituents	Nitroaromatic compound - Benzenoid - Sulfone - Organoheterocyclic compound - Propargyl-type 1,3-dipolar organic compound - Organic oxoazanium - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organonitrogen compound - Aromatic heteropolycyclic compound
Description	This compound belongs to the class of organic compounds known as nitroaromatic compounds. These are c-nitro compounds where the nitro group is C-substituted with an aromatic group.
External Descriptors	C-nitro compound - sulfone - 1-benzothiophenes
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

3D Structure

Associated Targets(Human)

HIF1A Tchem Hypoxia-inducible factor 1-alpha (1 Activities)

Discover Target: HIF1A

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

VDR Tclin Vitamin D receptor (26531 Activities)

Discover Target: VDR

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

SRC Tclin Tyrosine-protein kinase SRC (10310 Activities)

Discover Target: SRC

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

APP Tclin Amyloid-beta A4 protein (8510 Activities)

Discover Target: APP

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ARSA Tbio Cerebroside-sulfatase (655 Activities)

Discover Target: ARSA

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

JAK2 Tclin Tyrosine-protein kinase JAK2 (12915 Activities)

Discover Target: JAK2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

MTOR Tclin Serine/threonine-protein kinase mTOR (13850 Activities)

Discover Target: MTOR

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

STAT3 Tchem Signal transducer and activator of transcription 3 (3313 Activities)

Discover Target: STAT3

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

DU-145 (51482 Activities)

Lot Number	Certificate Type	Date	Item
H2223521	Certificate of Analysis	Mar 11, 2026	S129623
H2223523	Certificate of Analysis	Mar 11, 2026	S129623
C2606544	Certificate of Analysis	Feb 06, 2026	S129623
C2606545	Certificate of Analysis	Feb 06, 2026	S129623
C2606572	Certificate of Analysis	Feb 06, 2026	S129623
C2606573	Certificate of Analysis	Feb 06, 2026	S129623
L2510110	Certificate of Analysis	Dec 16, 2025	S129623
K2328088	Certificate of Analysis	Sep 08, 2025	S129623
A2206700	Certificate of Analysis	Jul 15, 2025	S129623
C2512631	Certificate of Analysis	Oct 11, 2024	S129623
C2512635	Certificate of Analysis	Oct 11, 2024	S129623
C2512640	Certificate of Analysis	Oct 11, 2024	S129623
C2512641	Certificate of Analysis	Oct 11, 2024	S129623
C2512642	Certificate of Analysis	Oct 11, 2024	S129623
F2220028	Certificate of Analysis	Apr 02, 2024	S129623
E1718062	Certificate of Analysis	Jan 11, 2023	S129623

Solubility	DMSO 42 mg/mL Water <1 mg/mL Ethanol <1 mg/mL
Refractive Index	1.67
Boil Point(°C)	461.1° C
Melt Point(°C)	186 - 188 °C
Molecular Weight	211.200 g/mol
XLogP3	0.700
Hydrogen Bond Donor Count	0
Hydrogen Bond Acceptor Count	4
Rotatable Bond Count	0
Exact Mass	210.994 Da
Monoisotopic Mass	210.994 Da
Topological Polar Surface Area	88.300 Å²
Heavy Atom Count	14
Formal Charge	0
Complexity	375.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	0
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	1

Stattic - Moligand™,≥98% , CAS No.19983-44-9

Why this grade

Storage & shipping

Quality documents

Literature proof

Overview

Specifications

Documentation

📋 Safety Data Sheet (SDS)

✅ Certificate of Analysis (COA)

📊 Datasheet

🔬 Specification Sheet

Advanced Data

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