Bis(sulfur Dioxide)-1,4-diazabicyclo[2.2.2]octane Adduct - ≥95% , CAS No.119752-83-9

CAS: 119752-83-9 Cat. No.: D166360 Peso molecular: 240.3 Número EC: 802-457-9
Disponible para pedir
GRADE & PURITY ≥95%
Synonyms
1,4(c)\\diazabicyclo[2.2.2]octane(c)\\1,4(c)\\diium(c)\\1,4(c)\\disulfinate | 1,4-Diazabicyclo[2.2.2]octane bis(sulfur dioxide) | SY099324 | EN300-321062 | 1,4-Diazabicyclo[2.2.2]octane-1,4-diium-1,4-disulfinate | AMY34553 | Z2689031572 | 1,4-Diazoniabicy
Storage
Store at 2-8°C,Argon charged
Shipped In
Wet ice
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
1g
D166360-1g
1

14,90US$

22,90US$
Guardar 8,00 US$ (34.93%)
5g
D166360-5g
1

17,90US$

26,90US$
Guardar 9,00 US$ (33.46%)
25g
D166360-25g
1

56,90US$

85,90US$
Guardar 29,00 US$ (33.76%)
Enter a quantity for the sizes you want to add.
🧪

Why this grade

≥95% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at 2-8°C,Argon charged Ships Wet ice 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 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

1,4-Diazabicyclo[2.2.2]octane bis(sulfur dioxide) (DABSO) is a charge transfer complex that can be used as a sulfur dioxide surrogate:

· In palladium-catalyzed aminosulfonylation process.

· In reaction with aryl bromides to synthesize sodium aryl sulfinates.

It can also be used to activate DMSO and o-vinylanilines for the synthesis of N-aryl-1H-benzo[d]imidazol-1-amine and 4-aryl quinolines, respectively

Specifications

Sinónimos
1, 4(c)\\diazabicyclo[2.2.2]octane(c)\\1, 4(c)\\diium(c)\\1, 4(c)\\disulfinate | 1, 4-Diazabicyclo[2.2.2]octane bis(sulfur dioxide) | SY099324 | EN300-321062 | 1, 4-Diazabicyclo[2.2.2]octane-1, 4-diium-1, 4-disulfinate | AMY34553 | Z2689031572 | 1, 4-Diazoniabicy
Especificaciones y pureza
≥95%
Condiciones de almacenamiento de almacenamiento
Store at 2-8°C, Argon charged
Enviado en
Wet ice
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Pureza
≥95%
Nombres e identificadores
Sonrisas canónicasC1C[N+]2(CC[N+]1(CC2)S(=O)[O-])S(=O)[O-]
IUPAC Name1,4-diazoniabicyclo[2.2.2]octane-1,4-disulfinate
InChIKeyRWISEVUOFYXWFO-UHFFFAOYSA-N
INCHI1S/C6H12N2O4S2/c9-13(10)7-1-2-8(5-3-7,6-4-7)14(11)12/h1-6H2
Isómeros SMILES C1C[N+]2(CC[N+]1(CC2)S(=O)[O-])S(=O)[O-]
WGK Alemania 3
Peso molecular 240.3
Reaxy-Rn 21980336
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=21980336&ln=

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

KingdomOrganic compounds
SuperclassOrganoheterocyclic compounds
ClaseDiazinanes
SubclassPiperazines
Intermediate Tree Nodes Not available
Direct ParentN-alkylpiperazines
Alternative Parents Azacyclic compounds  Organopnictogen compounds  Organonitrogen compounds  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAliphatic heteropolycyclic compounds
Substituents N-alkylpiperazine - Azacycle - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organonitrogen compound - Aliphatic heteropolycyclic compound
DescripciónThis compound belongs to the class of organic compounds known as n-alkylpiperazines. These are organic compounds containing a piperazine ring where the nitrogen ring atom carries an alkyl group.
External Descriptors Not available
Estructura 3D
Modelo de Estructura Química Interactiva





Certificados (CoA, COO, BSE/TSE y tabla de análisis)
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.

8 results found

Lot NumberCertificate TypeFechaArticulo
J2326295Certificate of AnalysisAug 11, 2025 D166360
J2326296Certificate of AnalysisAug 11, 2025 D166360
J2326299Certificate of AnalysisAug 11, 2025 D166360
J2531460Certificate of AnalysisApr 28, 2024 D166360
J2531459Certificate of AnalysisApr 28, 2024 D166360
K2117704Certificate of AnalysisSep 14, 2023 D166360
K2117705Certificate of AnalysisSep 14, 2023 D166360
J2409209Certificate of AnalysisSep 12, 2023 D166360
Propiedades químicas y físicas
SolubilidadSoluble in water
Sensibilidadair and heat and moisture sensitive
Punto de fusión (°C)180 °C
Peso molecular240.300 g/mol
XLogP3-2.100
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count6
Rotatable Bond Count0
Exact Mass240.024 Da
Monoisotopic Mass240.024 Da
Topological Polar Surface Area119.000 Ų
Heavy Atom Count14
Formal Charge0
Complexity243.000
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
Preguntas frecuentes y artículos
Citations of This Product
Referencias
1. Wei Xiao, Jian-Qiang Chen, Jie Wu.  (2025)  Radical sulfonylation with sulfur dioxide surrogates.  CHEMICAL SOCIETY REVIEWS,      [PMID:40498470] [10.1039/D4CS01312C]
Calculadoras de soluciones
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