(R)-2-amino-3-(5-chlorothiophen-2-yl)propanoic acid CAS 1151862-89-3

Purity 97%+In StockPharmaceutical Standards
CAS No.1151862-89-3
Molecular FormulaC7H8ClNO2S
Molecular Weight205.66 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(R)-2-amino-3-(5-chlorothiophen-2-yl)propanoic acid CAS 1151862-89-3 chemical structure

Description

CATO manufactures (R)-2-amino-3-(5-chlorothiophen-2-yl)propanoic acid under ISO 17034:2016 accreditation with dual CNAS and ANAB accreditation. Each batch is characterized by orthogonal methods and supplied with a full Certificate of Analysis (COA), ensuring metrological traceability.

(R)-2-amino-3-(5-chlorothiophen-2-yl)propanoic acid (CAS 1151862-89-3), molecular formula C7H8ClNO2S and molecular weight 205.66 g/mol, is a CATO reference standard with documented purity and traceability.

Owing to an amide group, a sulfone group, a carboxylic acid group, a hydroxyl group, an ether linkage, chlorine substitution, an aromatic ring system, (R)-2-amino-3-(5-chlorothiophen-2-yl)propanoic acid is typically off-white to pale yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 205.66 g/mol — guide the selection of appropriate sample preparation and analytical techniques. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

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

Physical & Chemical Properties

Molecular FormulaC7H8ClNO2S
Molecular Weight205.66 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in methanol, acetonitrile, DMSO, water (slightly soluble)
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1989
Halogen ContentCl-containing
Nitrogen Atoms1
Sulfur Atoms1

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