Sodium xylenesulfonate solution - mixture of isomers, 40wt. % in H₂O , CAS No.1300-72-7

CAS: 1300-72-7 Cat. No.: S485589 Fórmula: (CH₃)₂C₆H₃SO₃Na Peso molecular: 208.21 Número CE: 215-090-9 PubChem CID: 23668192

GRADE & PURITY mixture of isomers, 40wt. % in H₂O

Synonyms

UNII-2OYF82G7KK | Richonate SXS | sodium 4-o-xylene sulfonate | Tox21_111000 | sodium 3,4-dimethylbenzenesulfonate | CAPECITABINE [WHO-DD] | QUCDWLYKDRVKMI-UHFFFAOYSA-M | J-005743 | VS-08577 | Xylenesulfonic acid, sodium salt | Z2740003284 | Benzenesulfon

Storage

Room temperature

Visão geral

Description

Sodium xylenesulfonate solution may be used in chemical synthesis studies.

Specifications

Sinónimos

UNII-2OYF82G7KK | Richonate SXS | sodium 4-o-xylene sulfonate | Tox21_111000 | sodium 3,4-dimethylbenzenesulfonate | CAPECITABINE [WHO-DD] | QUCDWLYKDRVKMI-UHFFFAOYSA-M | J-005743 | VS-08577 | Xylenesulfonic acid, sodium salt | Z2740003284 | Benzenesulfon

Especificações e pureza

mixture of isomers, 40wt. % in H₂O

Condições de armazenamento de armazenamento

Room temperature

Nomes e identificadores

Pubchem Sid

504769549

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/504769549

Sorrisos canónicos

CC1=C(C=C(C=C1)S(=O)(=O)[O-])C.[Na+]

IUPAC Name

sodium;3,4-dimethylbenzenesulfonate

InChIKey

QUCDWLYKDRVKMI-UHFFFAOYSA-M

INCHI

1S/C8H10O3S.Na/c1-6-3-4-8(5-7(6)2)12(9,10)11;/h3-5H,1-2H3,(H,9,10,11);/q;+1/p-1

SMILES isoméricas

CC1=C(C=C(C=C1)S(=O)(=O)[O-])C.[Na+]

WGK Alemanha

1

RTECS

ZE5100000

PubChem CID

23668192

Peso molecular

208.21

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Classe Benzene and substituted derivatives
      • Subclass Benzenesulfonic acids and derivatives

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Classe: Benzene and substituted derivatives
• Subclass: Benzenesulfonic acids and derivatives
• Intermediate Tree Nodes: Not available
• Direct Parent: p-Methylbenzenesulfonates
• Alternative Parents: Benzenesulfonyl compounds 1-sulfo,2-unsubstituted aromatic compounds o-Xylenes Sulfonyls Organosulfonic acids Organic sodium salts Organic oxides Hydrocarbon derivatives Organic cations
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: P-methylbenzenesulfonate - Arylsulfonic acid or derivatives - Benzenesulfonyl group - 1-sulfo,2-unsubstituted aromatic compound - O-xylene - Xylene - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Organosulfonic acid - Sulfonyl - Organic alkali metal salt - Organic oxygen compound - Organosulfur compound - Organic salt - Organic sodium salt - Hydrocarbon derivative - Organic oxide - Organic cation - Aromatic homomonocyclic compound
• Descrição: This compound belongs to the class of organic compounds known as p-methylbenzenesulfonates. These are benzenesulfonic acids (or derivative thereof) carrying a methyl group at the para- position.
• External Descriptors: Not available

Data sources

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

Alvos associados (humanos)

NFKB1 Tclin Nuclear factor NF-kappa-B p105 subunit (1459 Activities)

Discover Target: NFKB1

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

LMNA Tbio Prelamin-A/C (36751 Activities)

Discover Target: LMNA

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

Alvos associados (não humanos)

Plasmodium falciparum (966862 Activities)

Explore this target

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

Nfe2l2 Nuclear factor erythroid 2-related factor 2 (214 Activities)

Discover Target: Nfe2l2

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

Mecanismos de ação

Propriedades químicas e físicas

• Peso molecular: 208.210 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 1
• Exact Mass: 208.017 Da
• Monoisotopic Mass: 208.017 Da
• Topological Polar Surface Area: 65.600 Ų
• Heavy Atom Count: 13
• Formal Charge: 0
• Complexity: 245.000
• 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: 2

XLogP3

Perguntas frequentes

How should this product be stored?

Store at room temperature.

What are the CAS number, molecular formula and molecular weight?

The CAS Number is 1300-72-7, the molecular formula is C8H9NaO3S, and the molecular weight is 208.21 g/mol. InChIKey QUCDWLYKDRVKMI-UHFFFAOYSA-M.

What documentation is provided?

Available product documentation, including Certificates of Analysis (COA), Safety Data Sheets (SDS), and specification sheets, is shown in the product document area. Document availability and access follow the current site policy.