(4-Carbamimidoylphenyl)methanesulfonyl fluoride hydrochloride(p-APMSF hydrochloride) - Moligand™,≥95% , CAS No.74938-88-8

CAS: 74938-88-8 Cat. No.: P1443847 Formula: C₈H₉FN₂O₂S · HCl Peso molecolare: 252.69 Beilstein Registry Number: 9083148

GRADE & PURITY Moligand™, ≥95%

Synonyms

APMSF HCL | (4-Carbamimidoylphenyl)methanesulfonyl fluoride hydrochloride | 4-Amidinophenylmethanesulfonyl Fluoride Hydrochloride | p-Amidinophenylmethylsulfonylfluoride hydrochloride | p-APMSF (hydrochloride) | p-APMSF | para-APMSF | (p-Amidinophenyl)met

Storage

Store at -20°C,Argon charged

Shipped In

Ice chest + Ice pads

Panoramica

p-APMSF is an irreversible inhibitor of serinase. p-APMSFhas substrate specificity for positively charged side chains of amino acids ,lysine, or arginine. p-APMSF can be used to study the irreversible inhibitionof trypsin and thrombin.

Specifications

Sinonimi

APMSF HCL | (4-Carbamimidoylphenyl)methanesulfonyl fluoride hydrochloride | 4-Amidinophenylmethanesulfonyl Fluoride Hydrochloride | p-Amidinophenylmethylsulfonylfluoride hydrochloride | p-APMSF (hydrochloride) | p-APMSF | para-APMSF | (p-Amidinophenyl)met

Specifiche e purezza

Moligand™,≥95%

Condizioni di conservazione di stoccaggio

Store at -20°C,Argon charged

Spedito in

Ice chest + Ice pads

Questo prodotto richiede spedizione a catena fredda. I servizi di terra e altri servizi economici non sono disponibili.

Grado

Moligand™

Tipo di azione

INHIBITOR

Purezza

≥95%

Nomi e identificatori

Sorrisi canonici

C1=CC(=CC=C1CS(=O)(=O)F)C(=N)N.Cl

IUPAC Name

(4-carbamimidoylphenyl)methanesulfonyl fluoride;hydrochloride

InChIKey

KHLLRHIUKOJXLL-UHFFFAOYSA-N

INCHI

1S/C8H9FN2O2S.ClH/c9-14(12,13)5-6-1-3-7(4-2-6)8(10)11;/h1-4H,5H2,(H3,10,11);1H

Isomeri SMILES

C1=CC(=CC=C1CS(=O)(=O)F)C(=N)N.Cl

CAS alternativo

71933-13-6（free）

Peso molecolare

252.69

Beilstein

9083148

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: Sulfonyls Sulfonyl fluorides Organosulfonic acids and derivatives Carboximidamides Carboxamidines Organic oxides Organic chloride salts Hydrochlorides Hydrocarbon derivatives Organic anions
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Monocyclic benzene moiety - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Sulfonyl fluoride - Sulfonyl halide - Sulfonyl - Amidine - Carboxylic acid amidine - Carboximidamide - Organic nitrogen compound - Organic oxygen compound - Hydrochloride - Organic chloride salt - Hydrocarbon derivative - Organosulfur compound - Organonitrogen compound - Organic oxide - Organic anion - 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

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

Proprietà chimiche e fisiche

• Sensibilità: Moisture sensitive