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1-Phenylprop-2-en-1-one (Contains stabilizer) - 95%, high purity , CAS No.768-03-6

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1-Phenylprop-2-en-1-one (Contains stabilizer) - 95%, high purity , CAS No.768-03-6

COA

Grade & Purity:

≥95%

Cas Number: 768-03-6
Molecular Weight: 132.16
MDL number: MFCD00457275
PubChem CID: 13028

In stock

Item Number

P304587

Grouped product items
SKU	Size	Availability	Price
P304587-100mg	100mg	2	$99.90
P304587-250mg	250mg	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$179.90
P304587-1g	1g	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$379.90
P304587-5g	5g	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$1,139.90

View related series

Aryl group (63) Organic building blocks (409)

Basic Description

Synonyms	Phenylvinyl ketone \| Acrylophenone \| SCHEMBL13158915 \| FT-0727567 \| Q20707278 \| 1-Phenyl-2-propen-1-one \| BDBM50444877 \| 2-Propenophenone \| UNII-O4QWF7V5AA \| 3Oxo3phenylpropene \| 3-Oxo-3-phenylpropene \| 1-PHENYL-2-PROPEN-1-ONE (STABILIZED WITH TBC) \| BS-1
Specifications & Purity	≥95%
Storage Temp	Protected from light,Store at -20°C,Argon charged
Shipped In	Ice chest + Ice pads This product requires cold chain shipping. Ground and other economy services are not available.
Product Description	1-Phenylprop-2-en-1-one(stabilized with TBC) is an active-site directed irreversible inhibitor of hydroxynitrile lyase. Product Application: 1-Phenyl-2-propen-1-one is a chemical reagent used in the synthesis of pharmaceutical agents. Used in the preparation of functionalized aminoindolizines as well as pyrano[3,2-x]coumarins.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Benzenoids
  - Class Benzene and substituted derivatives
    - Subclass Benzoyl derivatives

Kingdom	Organic compounds
Superclass	Benzenoids
Class	Benzene and substituted derivatives
Subclass	Benzoyl derivatives
Intermediate Tree Nodes	Not available
Direct Parent	Benzoyl derivatives
Alternative Parents	Aryl ketones Enones Acryloyl compounds Organic oxides Hydrocarbon derivatives
Molecular Framework	Aromatic homomonocyclic compounds
Substituents	Aryl ketone - Benzoyl - Alpha,beta-unsaturated ketone - Enone - Acryloyl-group - Ketone - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Aromatic homomonocyclic compound
Description	This compound belongs to the class of organic compounds known as benzoyl derivatives. These are organic compounds containing an acyl moiety of benzoic acid with the formula (C6H5CO-).
External Descriptors	Not available
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Associated Targets(Human)

PRKACA Tchem cAMP-dependent protein kinase alpha-catalytic subunit (3475 Activities)

Discover Target: PRKACA

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

AKT1 Tchem Serine/threonine-protein kinase AKT (9192 Activities)

Discover Target: AKT1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mechanisms of Action

Mechanism of Action	Action Type	target ID	Target Name	Target Type	Target Organism	Binding Site Name	References

Names and Identifiers

IUPAC Name	1-phenylprop-2-en-1-one
INCHI	InChI=1S/C9H8O/c1-2-9(10)8-6-4-3-5-7-8/h2-7H,1H2
InChIKey	KUIZKZHDMPERHR-UHFFFAOYSA-N
Smiles	C=CC(=O)C1=CC=CC=C1
Isomeric SMILES	C=CC(=O)C1=CC=CC=C1
PubChem CID	13028
Molecular Weight	132.16

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.

16 results found

Lot Number	Certificate Type	Date	Item
L2423145	Certificate of Analysis	Dec 16, 2024	P304587
L2423146	Certificate of Analysis	Dec 16, 2024	P304587
L2423147	Certificate of Analysis	Dec 16, 2024	P304587
L2423148	Certificate of Analysis	Dec 16, 2024	P304587
L2423149	Certificate of Analysis	Dec 16, 2024	P304587
L2423150	Certificate of Analysis	Dec 16, 2024	P304587
L2423266	Certificate of Analysis	Dec 16, 2024	P304587
L2423141	Certificate of Analysis	Dec 16, 2024	P304587
L2423265	Certificate of Analysis	Dec 16, 2024	P304587
G2509083	Certificate of Analysis	Dec 16, 2024	P304587
L2423142	Certificate of Analysis	Dec 16, 2024	P304587
L2423143	Certificate of Analysis	Dec 16, 2024	P304587
L2423144	Certificate of Analysis	Dec 16, 2024	P304587
L2325238	Certificate of Analysis	Dec 15, 2023	P304587
L2325242	Certificate of Analysis	Dec 15, 2023	P304587
L2325240	Certificate of Analysis	Dec 15, 2023	P304587

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Chemical and Physical Properties

Sensitivity	Light and heat sensitive
Flash Point(°C)	73.7°C
Boil Point(°C)	202.6°C at 760 mmHg
Molecular Weight	132.160 g/mol
XLogP3	1.900
Hydrogen Bond Donor Count	0
Hydrogen Bond Acceptor Count	1
Rotatable Bond Count	2
Exact Mass	132.058 Da
Monoisotopic Mass	132.058 Da
Topological Polar Surface Area	17.100 Å²
Heavy Atom Count	10
Formal Charge	0
Complexity	132.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	0
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	1

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