(1,4,5,6-Tetrahydrocyclopenta[c]pyrazol-3-yl)methanol CAS 1215295-82-1

Purity 97%+In StockPharmaceutical Standards
CAS No.1215295-82-1
Molecular FormulaC7H10N2O
Molecular Weight138.17 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(1,4,5,6-Tetrahydrocyclopenta[c]pyrazol-3-yl)methanol CAS 1215295-82-1 chemical structure

Description

The occurrence of (1,4,5,6-Tetrahydrocyclopenta[c]pyrazol-3-yl)methanol is closely related to an amide group, a hydroxyl group, an ether linkage, an aromatic ring system in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

(1,4,5,6-Tetrahydrocyclopenta[c]pyrazol-3-yl)methanol (CAS 1215295-82-1), molecular formula C7H10N2O and molecular weight 138.17 g/mol, is a CATO reference standard with documented purity and traceability.

Structurally, (1,4,5,6-Tetrahydrocyclopenta[c]pyrazol-3-yl)methanol (C7H10N2O) contains an amide 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 138.17 g/mol, it falls into the low-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.

As a certified reference material (CRM), (1,4,5,6-Tetrahydrocyclopenta[c]pyrazol-3-yl)methanol 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 FormulaC7H10N2O
Molecular Weight138.17 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)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1990
Nitrogen Atoms2

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