AB45089

122-00-9 | 4'-Methylacetophenone

Name: Name:4'-Methylacetophenone
Brand: A2BChem
SKU: AB45089
Availability: InStock
Rating: 96 (1 reviews)

Packsize	Purity	Availability	Price	Discounted Price	Quantity
100g	98%	in stock	$15.00	$10.00	- +
1kg	98%	in stock	$140.00	$98.00	- +
5kg	98%	in stock	$540.00	$378.00	- +
10kg	98%	in stock	$833.00	$583.00	- +
25kg	98%	in stock	$1,819.00	$1,273.00	- +
50kg	98%	in stock	$3,412.00	$2,388.00	- +
200kg	98%	in stock	$9,162.00	$6,413.00	- +

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Description

Catalog Number:	AB45089
Chemical Name:	4'-Methylacetophenone
CAS Number:	122-00-9
Molecular Formula:	C9H10O
Molecular Weight:	134.1751
MDL Number:	MFCD00008751
SMILES:	Cc1ccc(cc1)C(=O)C
NSC Number:	9401

Computed Properties

Complexity:	121
Covalently-Bonded Unit Count:	1
Heavy Atom Count:	10

Hydrogen Bond Acceptor Count:	1
Rotatable Bond Count:	1
XLogP3:	2.1

Upstream Synthesis Route

1-(p-Tolyl)ethanone, also known as p-Tolyl methyl ketone, is a valuable organic compound commonly used in various chemical synthesis processes. With its distinct aromatic structure and functional ketone group, this compound serves as a versatile building block in the production of a wide range of chemicals and materials.In chemical synthesis, 1-(p-Tolyl)ethanone plays a crucial role as a key intermediate in the manufacturing of pharmaceuticals, fragrances, and agrochemicals. Its presence in organic reactions enables the formation of complex molecules through processes such as condensation, oxidation, and reduction. The unique properties of this compound make it particularly useful in the creation of chiral compounds and asymmetric synthesis methodologies.Furthermore, 1-(p-Tolyl)ethanone serves as a precursor to various substituted derivatives with enhanced properties for specific applications. By introducing different functional groups to the molecule, chemists can tailor the reactivity and properties of the final products for desired purposes. This adaptability makes it an indispensable tool in the design and synthesis of new compounds with valuable industrial and scientific applications.

Literature

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[Broader substrate specifity of Candida parapsilosis SCR II for catalyzing acetophenone derivatives by site-directed mutagenesis].
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Characterization of the most odor-active compounds in an American Bourbon whisky by application of the aroma extract dilution analysis.
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Electronic effects of para-substitution on acetophenones in the reaction of rat liver 3alpha-hydroxysteroid dehydrogenase.
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Synthesis and in vivo evaluation of [18F]-4-[5-(4-methylphenyl)-3-(trifluoromethyl)-1H-pyrazol-1-yl]benzenesulfonamide as a PET imaging probe for COX-2 expression.
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Combined ruthenium(II) and lipase catalysis for efficient dynamic kinetic resolution of secondary alcohols. Insight into the racemization mechanism.
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Development of new synthetic methods with aryl 1-chlorovinyl sulfoxides.
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Keto-enol/enolate equilibria in the N-acetylamino-p-methylacetophenone system. Effect of a beta-nitrogen substituent.
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122-00-9 | 4'-Methylacetophenone