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5335-05-7

Chloromethyl benzoate

Catalog#: AR00DAB0  |   CAS#: 5335-05-7  |   MDL#: MFCD00040116  |   MF: C8H7ClO2  |   MW: 170.59297999999998

Packsize Purity Price Availability Quantity
250mg 98% $5.00 Global Stock Buy Now Add To Cart
1g 98% $5.00 Global Stock Buy Now Add To Cart
5g 98% $25.00 Global Stock Buy Now Add To Cart
10g 98% $49.00 Global Stock Buy Now Add To Cart
25g 98% $101.00 Global Stock Buy Now Add To Cart
100g 98% $362.00 Global Stock Buy Now Add To Cart
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Catalog Number AR00DAB0
Chemical Name Chloromethyl benzoate
CAS Number 5335-05-7
Molecular Formula C8H7ClO2
Molecular Weight 170.59297999999998
MDL Number MFCD00040116
SMILES ClCOC(=O)c1ccccc1
NSC Number 2876

Chloromethyl benzoate is a versatile chemical compound with valuable applications in chemical synthesis. This compound serves as a crucial building block in the creation of various organic molecules through its reactivity with nucleophiles. In particular, chloromethyl benzoate is commonly employed in the formation of esters, amides, and other organic derivatives.One prominent use of chloromethyl benzoate is in the modification of biologically active compounds to enhance their pharmaceutical properties. By reacting with functional groups on drug molecules, chloromethyl benzoate can introduce specific chemical motifs that improve the drug's solubility, stability, or targeting ability in the body. This process, known as derivatization, is essential in drug development to optimize therapeutic efficacy.Furthermore, chloromethyl benzoate plays a significant role in the synthesis of fragrances and flavoring agents. By incorporating this compound into aromatic compounds through esterification or amidation reactions, chemists can tailor the sensory properties of the final product. The presence of the benzoyl group in chloromethyl benzoate imparts a distinct odor and taste profile, making it a valuable precursor in the fragrance industry.In organic chemistry laboratories, chloromethyl benzoate is a valuable reagent for the preparation of starting materials for diverse synthetic pathways. Its ability to undergo nucleophilic substitution reactions makes it a versatile intermediate for the construction of complex molecules, including pesticides, polymers, and specialty chemicals. Researchers and synthetic chemists rely on the synthesis of chloromethyl benzoate to access a wide range of chemical structures for academic and industrial applications.
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GHS Pictogram
Signal Word Warning
UN# N/A
Hazard Statements H302-H315-H319-H335
Precautionary Statements P261-P305+P351+P338
Class N/A
Packing Group N/A

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