1-(tert-Butyl)-2-cyclopropoxy-3-fluorobenzene CAS 1243393-36-3

Purity 97%+In StockPharmaceutical Standards
CAS No.1243393-36-3
Molecular FormulaC13H17FO
Molecular Weight208.27 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-(tert-Butyl)-2-cyclopropoxy-3-fluorobenzene CAS 1243393-36-3 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 1-(tert-Butyl)-2-cyclopropoxy-3-fluorobenzene.

1-(tert-Butyl)-2-cyclopropoxy-3-fluorobenzene (CAS 1243393-36-3), molecular formula C13H17FO and molecular weight 208.27 g/mol, is a CATO reference standard with documented purity and traceability.

The molecular framework of 1-(tert-Butyl)-2-cyclopropoxy-3-fluorobenzene (C13H17FO) is characterized by a hydroxyl group, an ether linkage, fluorine substitution, an aromatic ring system. In reversed-phase chromatography, its retention is governed primarily by its high hydrophobicity (logP), which provides a practical basis for HPLC-UV/DAD or LC-MS method development. 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 1-(tert-Butyl)-2-cyclopropoxy-3-fluorobenzene 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 FormulaC13H17FO
Molecular Weight208.27 g/mol
Purity97%+
StorageStore at room temperature, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure
Degree of Unsaturation (DBE)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1990
Halogen ContentF-containing

Recommended Standards

Why CATO?