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LYSINE ACETYL-SALICYLATE

CAS 77337-52-1C15H22N2O6MW 326.34

LYSINE ACETYL-SALICYLATE (CAS 77337-52-1) — formula C15H22N2O6, molecular weight 326.34; category organic chemicals.

Product Overview

CAS Number77337-52-1
Molecular FormulaC15H22N2O6
Molecular Weight326.34
CategoryOrganic Chemicals

Technical Profile

What this product is

LYSINE ACETYL-SALICYLATE is a carbon-based organic compound with CAS registry number 77337-52-1 and molecular formula C15H22N2O6 (molecular weight 326.34), belonging to the organic chemicals segment of chemical raw materials.

Identification

CAS number: 77337-52-1

Its molecular formula C15H22N2O6 comprises 15 C, 22 H, 2 N, 6 O atoms.

Also known as: LYSINE ACETYL-SALICYLATE · 赖氨酸乙酰水杨酸盐

Category: organic chemicals

Frequently Asked Questions

What is the CAS number of LYSINE ACETYL-SALICYLATE?

The CAS registry number of LYSINE ACETYL-SALICYLATE is 77337-52-1.

What is the molecular formula and molecular weight of LYSINE ACETYL-SALICYLATE?

Molecular formula C15H22N2O6, molecular weight 326.34.

What other names is LYSINE ACETYL-SALICYLATE known by?

It is also registered under: LYSINE ACETYL-SALICYLATE, 赖氨酸乙酰水杨酸盐.

Which category does LYSINE ACETYL-SALICYLATE belong to?

Category: Organic Chemicals.

PubChem Public Data

Independent reference data for LYSINE ACETYL-SALICYLATE (CAS 77337-52-1), compiled from public chemistry databases.

Registry identifiers across databases

CAS Registry Number77337-52-1
PubChem CID91626
Molecular formulaC15H22N2O6
IUPAC name2-acetyloxybenzoic acid;(2S)-2,6-diaminohexanoic acid
UNII (FDA)XAN4V337CI

Computed descriptors

Molecular Weight326.34
Hydrogen Bond Donor Count4
Hydrogen Bond Acceptor Count8
Rotatable Bond Count8
Exact Mass326.14778643
Monoisotopic Mass326.14778643
Topological Polar Surface Area153
Heavy Atom Count23

Documented uses on record

    Compounds capable of relieving pain without the loss of CONSCIOUSNESS.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

    acetylsalicylic acid lysinate; Flectadol; aspirin lysine; aspirin lysinate; XAN4V337CI; L-lysine, 2-(acetyloxy)benzoate (1:1); lysine-aspirin; Asprin DL-Lysine; lysine-acetylsalicylic acid; RefChem:916390; 253-723-0; Solusprin; 37933-78-1; 2-acetyloxybenzoic acid;(2S)-2,6-diaminohexanoic acid; L-Lysine compound with 2-acetoxybenzoic acid (1:1); L-lysine acetylsalicylate

    What the public record says

    LYSINE ACETYL-SALICYLATE · CAS 77337-52-1 · C15H22N2O6. UNII XAN4V337CI.

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

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