4-((Trimethylsilyl)ethynyl)-7H-pyrrolo[2,3-d]pyrimidine CAS 1147014-68-3

Purity 97%+In StockPharmaceutical Standards
CAS No.1147014-68-3
Molecular FormulaC11H13N3Si
Molecular Weight215.33 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-((Trimethylsilyl)ethynyl)-7H-pyrrolo[2,3-d]pyrimidine CAS 1147014-68-3 chemical structure

Description

Under current pharmacopoeial and regulatory frameworks, quality-control requirements for this class of reference material explicitly involve the control of targets including 4-((Trimethylsilyl)ethynyl)-7H-pyrrolo[2,3-d]pyrimidine.

CATO supplies 4-((Trimethylsilyl)ethynyl)-7H-pyrrolo[2,3-d]pyrimidine (CAS 1147014-68-3), a certified reference material (molecular formula C11H13N3Si, MW 215.33 g/mol) for analytical method development and quality control.

4-((Trimethylsilyl)ethynyl)-7H-pyrrolo[2,3-d]pyrimidine (C11H13N3Si) contains a nitrogen-containing heterocyclic scaffold, a nitrile group. Its high carbon-to-hydrogen ratio confers good lipid solubility; these physicochemical properties determine the optimal preparation and storage of its standard solutions. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

This reference standard is suitable for quantitative analysis on major chromatographic platforms including HPLC, GC, LC-MS/MS, and GC-MS, serving as an external calibration standard or a system suitability test reference material.

As a certified reference material (CRM), 4-((Trimethylsilyl)ethynyl)-7H-pyrrolo[2,3-d]pyrimidine 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 FormulaC11H13N3Si
Molecular Weight215.33 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)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1989
Nitrogen Atoms3

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