4-(Benzyloxy)benzyl chloride

98%

Reagent Code: #144485
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CAS Number 836-42-0

science Other reagents with same CAS 836-42-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 232.71 g/mol
Formula C₁₄H₁₃ClO
badge Registry Numbers
MDL Number MFCD00000916
inventory_2 Storage & Handling
Storage 2~8℃

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals. Its reactive chloride group allows for nucleophilic substitution reactions, enabling the introduction of the 4-(benzyloxy)benzyl moiety into larger molecules. Commonly employed in the synthesis of antiviral and anticancer agents due to its ability to act as a building block for more complex structures. Also utilized in the development of protected benzyl derivatives for use in peptide and carbohydrate chemistry. The benzyloxy group serves as a protecting group for phenols, facilitating selective reactions in multi-step syntheses.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿1,150.00
5g
10-20 days ฿4,420.00
25g
10-20 days ฿13,250.00

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4-(Benzyloxy)benzyl chloride
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals. Its reactive chloride group allows for nucleophilic substitution reactions, enabling the introduction of the 4-(benzyloxy)benzyl moiety into larger molecules. Commonly employed in the synthesis of antiviral and anticancer agents due to its ability to act as a building block for more complex structures. Also utilized in the development of protected benzyl derivatives for use in peptide and

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals. Its reactive chloride group allows for nucleophilic substitution reactions, enabling the introduction of the 4-(benzyloxy)benzyl moiety into larger molecules. Commonly employed in the synthesis of antiviral and anticancer agents due to its ability to act as a building block for more complex structures. Also utilized in the development of protected benzyl derivatives for use in peptide and carbohydrate chemistry. The benzyloxy group serves as a protecting group for phenols, facilitating selective reactions in multi-step syntheses.

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