Name: Fenile disolfuro - ≥99% , CAS No.882-33-7
SKU: P101812
Availability: InStock

Fenile disolfuro - ≥99% , CAS No.882-33-7

CAS: 882-33-7 Cat. No.: P101812 Formula: C₆H₅SSC₆H₅ Peso molecolare: 218.34 Beilstein Registry Number: 639794 Numero EC: 212-926-4

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Disponibile su ordine

GRADE & PURITY ≥99%

Synonyms

Storage

Room temperature

Shipped In

Normale

Panoramica Specifications Nomi e identificatori Documentazione Advanced Data Taxonomic Classification Struttura 3D Obiettivi associati (umani) Obiettivi associati (non umani) Meccanismi d'azione Certificati (CoA, COO, BSE/TSE e tabella di analisi) Proprietà chimiche e fisiche Domande frequenti e articoli Citations of This Product Calcolatori di soluzioni Recensioni

🧪

Why this grade

≥99% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Room temperature Ships Normale Check lot-specific COA for exact specifications.

📋

Quality documents

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

📚

Literature proof

Cited in 15 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Panoramica

È il prodotto di idrolisi del disfonato (insetticida) e partecipa all'idrolizzazione degli alchini attraverso un meccanismo di trasferimento di elettroni singoli mediato dalle ammine.

Specifications

Sinonimi

Specifiche e purezza

≥99%

Condizioni di conservazione di stoccaggio

Room temperature

Spedito in

Normale

Purezza

≥99%

Nomi e identificatori

Pubchem Sid

504752451

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/504752451

Sorrisi canonici

C1=CC=C(C=C1)SSC2=CC=CC=C2

IUPAC Name

(phenyldisulfanyl)benzene

InChIKey

GUUVPOWQJOLRAS-UHFFFAOYSA-N

INCHI

1S/C12H10S2/c1-3-7-11(8-4-1)13-14-12-9-5-2-6-10-12/h1-10H

Isomeri SMILES

C1=CC=C(C=C1)SSC2=CC=CC=C2

WGK Germania

RTECS

SS6825000

Numero UN

3335

Peso molecolare

218.34

Beilstein

639794

Reaxy-Rn

639794

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=639794&ln=

Documentazione

📋 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 Benzenoids
  - Classe Benzene and substituted derivatives

Kingdom	Organic compounds
Superclass	Benzenoids
Classe	Benzene and substituted derivatives
Subclass	Not available
Intermediate Tree Nodes	Not available
Direct Parent	Benzene and substituted derivatives
Alternative Parents	Organic disulfides Sulfenyl compounds Hydrocarbon derivatives
Molecular Framework	Aromatic homomonocyclic compounds
Substituents	Monocyclic benzene moiety - Organic disulfide - Sulfenyl compound - Hydrocarbon derivative - Organosulfur compound - Aromatic homomonocyclic compound
Descrizione	This compound belongs to the class of organic compounds known as benzene and substituted derivatives. These are aromatic compounds containing one monocyclic ring system consisting of benzene.
External Descriptors	Not available
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

Struttura 3D

Obiettivi associati (umani)

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

PLK1 Tchem Serine/threonine-protein kinase PLK1 (28605 Activities)

Discover Target: PLK1

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

FBP1 Tchem Fructose-1,6-bisphosphatase (1199 Activities)

Discover Target: FBP1

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

MGLL Tchem Monoglyceride lipase (1909 Activities)

Discover Target: MGLL

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

HSD17B10 Tchem Endoplasmic reticulum-associated amyloid beta-peptide-binding protein (20669 Activities)

Discover Target: HSD17B10

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

POLI Tchem DNA polymerase iota (116820 Activities)

Discover Target: POLI

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

KDM4A Tchem Lysine-specific demethylase 4A (52245 Activities)

Discover Target: KDM4A

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

TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)

Discover Target: TDP1

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

ERG Tbio Transcriptional regulator ERG (5589 Activities)

Discover Target: ERG

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

SMN1 Tchem Survival motor neuron protein (34246 Activities)

Discover Target: SMN1

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

HPGD Tchem 15-hydroxyprostaglandin dehydrogenase [NAD+] (24926 Activities)

Discover Target: HPGD

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

GMNN Tbio Geminin (128009 Activities)

Discover Target: GMNN

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

CBX1 Tbio Chromobox protein homolog 1 (92434 Activities)

Discover Target: CBX1

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

Obiettivi associati (non umani)

Plasmodium falciparum (966862 Activities)

Explore this target

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

Luciferin 4-monooxygenase (66902 Activities)

Explore this target

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

Txnrd1 Thioredoxin reductase 1, cytoplasmic (45279 Activities)

Discover Target: Txnrd1

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

Mapt Microtubule-associated protein tau (6 Activities)

Discover Target: Mapt

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

fba Putative fructose-1,6-bisphosphate aldolase (15559 Activities)

Discover Target: fba

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

ffp 4'-phosphopantetheinyl transferase ffp (24982 Activities)

Discover Target: ffp

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

FTL Ferritin light chain (43324 Activities)

Discover Target: FTL

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

Meccanismi d'azione

Certificati (CoA, COO, BSE/TSE e tabella di analisi)

C of A & Other Certificates(BSE/TSE, COO):

Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

18 results found

Lot Number	Certificate Type	Data	Oggetto
D2627014	Certificate of Analysis	Apr 29, 2026	P101812
D2621089	Certificate of Analysis	Apr 28, 2026	P101812
A2628101	Certificate of Analysis	Feb 07, 2026	P101812
K2526160	Certificate of Analysis	Nov 28, 2025	P101812
A2207279	Certificate of Analysis	Oct 13, 2025	P101812
A2207281	Certificate of Analysis	Oct 13, 2025	P101812
A2207280	Certificate of Analysis	Oct 13, 2025	P101812
A2207278	Certificate of Analysis	Oct 13, 2025	P101812
C2127102	Certificate of Analysis	Jan 13, 2025	P101812
C2127103	Certificate of Analysis	Jan 13, 2025	P101812
C2127104	Certificate of Analysis	Jan 13, 2025	P101812
B2520539	Certificate of Analysis	Jul 16, 2024	P101812
E1923112	Certificate of Analysis	Mar 09, 2023	P101812
G1825229	Certificate of Analysis	May 09, 2022	P101812
B2514063	Certificate of Analysis	Dec 02, 2021	P101812
F2425028	Certificate of Analysis	Dec 02, 2021	P101812
F2520048	Certificate of Analysis	Dec 02, 2021	P101812
G2510043	Certificate of Analysis	Dec 02, 2021	P101812

Proprietà chimiche e fisiche

Solubilità	Insoluble in water.
Punto di ebollizione (°C)	310℃
Punto di fusione (°C)	58-60°C
Peso molecolare	218.300 g/mol
XLogP3	4.400
Hydrogen Bond Donor Count	0
Hydrogen Bond Acceptor Count	2
Rotatable Bond Count	3
Exact Mass	218.022 Da
Monoisotopic Mass	218.022 Da
Topological Polar Surface Area	50.600 Å²
Heavy Atom Count	14
Formal Charge	0
Complexity	128.000
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

Domande frequenti e articoli

Synthesis Strategy of Pentafluorothio Group - Synthesis of Aliphatic Compounds Containing SF₅

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Field of medicinal chemistry Fluorinated block Materials Science Halogenation Reagents Pentafluorosulfide Fluorination Reagent Pentafluorosulfidation Reaction Photocatalytic Reaction

Citations of This Product

How to Cite Aladdin Scientific Products? Citations Search

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Recensioni

📚 Citations by Application

Polymer synthesis & polymerization2

Organic synthesis — reaction medium11

Extraction & workup solvent5

Spectroscopy sample preparation2

Electrochemistry & battery electrolyte2

Other applications4

Drug / compound screening2

Cancer cell line characterization1

Industrial & non-pharma application1

View all 15 citations →

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