3-(2-Biphenyl)-2-chloro-1-propene CAS 951889-99-9

Purity 97%+In StockPharmaceutical Standards
CAS No.951889-99-9
Molecular FormulaC15H13Cl
Molecular Weight228.72 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-(2-Biphenyl)-2-chloro-1-propene CAS 951889-99-9 chemical structure

Description

The occurrence of 3-(2-Biphenyl)-2-chloro-1-propene is closely related to chlorine substitution, a polycyclic aromatic system in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

CATO supplies 3-(2-Biphenyl)-2-chloro-1-propene (CAS 951889-99-9), a certified reference material (molecular formula C15H13Cl, MW 228.72 g/mol) for analytical method development and quality control.

3-(2-Biphenyl)-2-chloro-1-propene (C15H13Cl) contains chlorine substitution, a polycyclic aromatic system. Halogen substitution raises its density and boiling point, 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.

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 3-(2-Biphenyl)-2-chloro-1-propene 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 FormulaC15H13Cl
Molecular Weight228.72 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Halogen ContentCl-containing

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