tert-Butyl 1,2,3-thiadiazol-5-ylcarbamate CAS 372089-60-6

Purity 97%+In StockPharmaceutical Standards
CAS No.372089-60-6
Molecular FormulaC7H11N3O2S
Molecular Weight201.25 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

tert-Butyl 1,2,3-thiadiazol-5-ylcarbamate CAS 372089-60-6 chemical structure

Description

The occurrence of tert-Butyl 1,2,3-thiadiazol-5-ylcarbamate is closely related to an amide group, a sulfone group, a carboxylic acid group, a hydroxyl group, an ether linkage, an aromatic ring system in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

CATO supplies tert-Butyl 1,2,3-thiadiazol-5-ylcarbamate (CAS 372089-60-6), a certified reference material (molecular formula C7H11N3O2S, MW 201.25 g/mol) for analytical method development and quality control.

Structurally, tert-Butyl 1,2,3-thiadiazol-5-ylcarbamate (C7H11N3O2S) contains an amide group, a sulfone group, a carboxylic acid group, a hydroxyl group, an ether linkage, an aromatic ring system. The molecule exhibits a degree of unsaturation (DBE) of 4.0, corresponding to approximately 4 ring(s) or double-bond equivalent(s). With a molecular weight of 201.25 g/mol, it falls into the medium-molecular-weight range. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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

CATO manufactures tert-Butyl 1,2,3-thiadiazol-5-ylcarbamate 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.

Physical & Chemical Properties

Molecular FormulaC7H11N3O2S
Molecular Weight201.25 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Nitrogen Atoms3
Sulfur Atoms1

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