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Alclofenac

CAS 22131-79-9C11H11ClO3MW 226.65

Alclofenac (CAS 22131-79-9) — formula C11H11ClO3, molecular weight 226.65.

Product Overview

CAS Number22131-79-9
Molecular FormulaC11H11ClO3
Molecular Weight226.65
LogP2.97
ApplicationsUse Classification: Pharmaceuticals

Applications

Documented applications: Use Classification: Pharmaceuticals.

Technical Profile

What this product is

Alclofenac is a chemical compound with CAS registry number 22131-79-9 and molecular formula C11H11ClO3 (molecular weight 226.65).

Identification

CAS number: 22131-79-9

Its molecular formula C11H11ClO3 comprises 11 C, 11 H, 1 Cl, 3 O atoms.

Also known as: Alclofenac · 阿氯芬酸

Frequently Asked Questions

What is the CAS number of Alclofenac?

The CAS registry number of Alclofenac is 22131-79-9.

What is the molecular formula and molecular weight of Alclofenac?

Molecular formula C11H11ClO3, molecular weight 226.65.

What other names is Alclofenac known by?

It is also registered under: Alclofenac, 阿氯芬酸.

What are the documented applications of Alclofenac?

Recorded applications: Use Classification: Pharmaceuticals.

PubChem Public Data

Independent reference data for Alclofenac (CAS 22131-79-9), compiled from public chemistry databases.

Registry identifiers across databases

CAS Registry Number22131-79-9
PubChem CID30951
Molecular formulaC11H11ClO3
IUPAC name2-(3-chloro-4-prop-2-enoxyphenyl)acetic acid
UNII (FDA)M9CP5H21N8

Computed descriptors

Molecular Weight226.65
XLogP32.5
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count3
Rotatable Bond Count5
Exact Mass226.0396719
Monoisotopic Mass226.0396719
Topological Polar Surface Area46.5
Heavy Atom Count15

Physicochemical values on record

LogP2.97

Documented uses on record

    Alclofenac is indicated in rheumatology, in particular for the treatment of rheumatoid arthritis, ankylosing spondylitis and, as an analgesic, in painful arthritic pathologies.Anti-inflammatory agents that are non-steroidal in nature. In addition to anti-inflammatory actions, they have analgesic, antipyretic, and platelet-inhibitory actions. They act by blocking the synthesis of prostaglandins by inhibiting cyclooxygenase, which converts arachidonic acid to cyclic endoperoxides, precursors of prostaglandins. Inhibition of prostaglandin synthesis accounts for their analgesic, antipyretic, and platelet-inhibitory actions; other mechanisms may contribute to their anti-inflammatory effects.

    Synonyms and trade names

    alclofenac; 22131-79-9; Medifenac; Prinalgin; Mervan; Alclophenac; Allopydin; Reufenac; Neosten; Neoston; Zumaril; Alclofenaco; Epinal; Alclofenacum; [4-(Allyloxy)-3-chlorophenyl]acetic acid; W 7320

    GHS hazard classification

    Reported hazard statementsH302 (100%)

    H302 (100%): Harmful if swallowed [Warning Acute toxicity, oral]

    P264, P270, P301+P317, P330, and P501 (click each P-code to see the statement)

    What the public record says

    Alclofenac · CAS 22131-79-9 · C11H11ClO3. UNII M9CP5H21N8. LogP: 2.97.

    Source: PubChem / Wikidata; the batch COA governs where values differ.

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