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4-Fluorocinnamaldehyde - ≥93%, high purity , CAS No.24654-55-5

    Grade & Purity:
  • ≥93%
In stock
Item Number
F736756
Grouped product items
SKU Size
Availability
Price Qty
F736756-1g
1g
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$9.90
F736756-5g
5g
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$26.90
F736756-25g
25g
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$66.90

Basic Description

Synonyms p-Fluorocinnamaldehyde | 3-(4-Fluorophenyl)acrylaldehyde | 3-(4-Fluorophenyl)-2-propenal
Specifications & Purity ≥93%
Storage Temp Store at 2-8°C,Argon charged
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Phenylpropanoids and polyketides
Class Cinnamaldehydes
Subclass Not available
Intermediate Tree Nodes Not available
Direct Parent Cinnamaldehydes
Alternative Parents Styrenes  Fluorobenzenes  Aryl fluorides  Enals  Organofluorides  Organic oxides  Hydrocarbon derivatives  Aldehydes  
Molecular Framework Aromatic homomonocyclic compounds
Substituents Cinnamaldehyde - Styrene - Fluorobenzene - Halobenzene - Aryl fluoride - Aryl halide - Monocyclic benzene moiety - Benzenoid - Enal - Alpha,beta-unsaturated aldehyde - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Carbonyl group - Organohalogen compound - Organofluoride - Organooxygen compound - Aldehyde - Aromatic homomonocyclic compound
Description This compound belongs to the class of organic compounds known as cinnamaldehydes. These are organic aromatic compounds containing a cinnamlaldehyde moiety, consisting of a benzene and an aldehyde group to form 3-phenylprop-2-enal.
External Descriptors Not available

Names and Identifiers

IUPAC Name (E)-3-(4-fluorophenyl)prop-2-enal
INCHI InChI=1S/C9H7FO/c10-9-5-3-8(4-6-9)2-1-7-11/h1-7H/b2-1+
InChIKey YSIYEWBILJZDQH-OWOJBTEDSA-N
Smiles C1=CC(=CC=C1C=CC=O)F
Isomeric SMILES C1=CC(=CC=C1/C=C/C=O)F
Molecular Weight 150.15
Reaxy-Rn 2078813
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2078813&ln=

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

5 results found

Lot Number Certificate Type Date Item
F2516254 Certificate of Analysis Jun 25, 2025 F736756
F2516255 Certificate of Analysis Jun 25, 2025 F736756
F2516256 Certificate of Analysis Jun 25, 2025 F736756
F2516258 Certificate of Analysis Jun 25, 2025 F736756
F2516259 Certificate of Analysis Jun 25, 2025 F736756

Chemical and Physical Properties

Sensitivity Air Sensitive,Heat Sensitive
Refractive Index 1.6
Flash Point(°C) 91 °C
Boil Point(°C) 95°C/2mmHg
Molecular Weight 150.150 g/mol
XLogP3 1.900
Hydrogen Bond Donor Count 0
Hydrogen Bond Acceptor Count 2
Rotatable Bond Count 2
Exact Mass 150.048 Da
Monoisotopic Mass 150.048 Da
Topological Polar Surface Area 17.100 Ų
Heavy Atom Count 11
Formal Charge 0
Complexity 146.000
Isotope Atom Count 0
Defined Atom Stereocenter Count 0
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 1
Undefined Bond Stereocenter Count 0
The total count of all stereochemical bonds 1
Covalently-Bonded Unit Count 1

Citations of This Product

1. Yangyang Zhou, Chen Chen, Qiling Li, Yanbo Liu, Ting Wei, Youzhen Liu, Zebing Zeng, Darren Bradshaw, Bing Zhang, Jia Huo.  (2022)  Precise control of selective hydrogenation of α,β-unsaturated aldehydes in water mediated by ammonia borane.  APPLIED CATALYSIS B-ENVIRONMENTAL,  311  (121348). 
2. Shuibo Wang, Biao Wu, Qiuju Zhang, Yiming Li, Lin Zhu, Hongbo Yu, Hongfeng Yin.  (2024)  Design of Pt@Sn core–shell nanocatalysts for highly selective hydrogenation of cinnamaldehyde to prepare cinnamyl alcohol.  CHEMICAL ENGINEERING JOURNAL,  488  (151019). 

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