[3-(thiophen-3-yl)-1,2,4-oxadiazol-5-yl]methanamine CAS 1156232-02-8

Purity 97%+In StockPharmaceutical Standards
CAS No.1156232-02-8
Molecular FormulaC7H7N3OS
Molecular Weight181.21 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

[3-(thiophen-3-yl)-1,2,4-oxadiazol-5-yl]methanamine CAS 1156232-02-8 chemical structure

Description

The occurrence of [3-(thiophen-3-yl)-1,2,4-oxadiazol-5-yl]methanamine is closely related to an amide group, sulfur-containing functionality, a hydroxyl group, an ether linkage, an aromatic ring system in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

[3-(thiophen-3-yl)-1,2,4-oxadiazol-5-yl]methanamine (CAS 1156232-02-8), molecular formula C7H7N3OS and molecular weight 181.21 g/mol, is a CATO reference standard with documented purity and traceability.

[3-(thiophen-3-yl)-1,2,4-oxadiazol-5-yl]methanamine (C7H7N3OS) contains an amide group, sulfur-containing functionality, a hydroxyl group, an ether linkage, an aromatic ring system. Its physicochemical properties are representative of its class; these physicochemical properties determine the optimal preparation and storage of its standard solutions. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

As a certified reference material (CRM), [3-(thiophen-3-yl)-1,2,4-oxadiazol-5-yl]methanamine meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

Physical & Chemical Properties

Molecular FormulaC7H7N3OS
Molecular Weight181.21 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1989
Nitrogen Atoms3
Sulfur Atoms1

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