tert-Butyl 5-iodopentanoate

98%

Reagent Code: #153410
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CAS Number 56198-37-9

science Other reagents with same CAS 56198-37-9

blur_circular Chemical Specifications

inventory_2 Storage & Handling
Storage 2-8°C, drying away from light

description Product Description

Used as an intermediate in organic synthesis, particularly in pharmaceutical and agrochemical manufacturing. The iodine atom serves as a good leaving group, enabling coupling reactions such as Suzuki or Stille cross-couplings. The ester group can be hydrolyzed to the corresponding carboxylic acid or reduced to an alcohol, allowing further functionalization. Commonly employed in the preparation of heterocyclic compounds and bioactive molecules where a five-carbon spacer with a terminal reactive site is needed. Its tert-butyl ester group offers stability under various reaction conditions and can be deprotected under acidic conditions when required.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿1,600.00
250mg
10-20 days ฿2,260.00
1g
10-20 days ฿5,930.00
5g
10-20 days ฿24,890.00
tert-Butyl 5-iodopentanoate
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Used as an intermediate in organic synthesis, particularly in pharmaceutical and agrochemical manufacturing. The iodine atom serves as a good leaving group, enabling coupling reactions such as Suzuki or Stille cross-couplings. The ester group can be hydrolyzed to the corresponding carboxylic acid or reduced to an alcohol, allowing further functionalization. Commonly employed in the preparation of heterocyclic compounds and bioactive molecules where a five-carbon spacer with a terminal reactive site is ne

Used as an intermediate in organic synthesis, particularly in pharmaceutical and agrochemical manufacturing. The iodine atom serves as a good leaving group, enabling coupling reactions such as Suzuki or Stille cross-couplings. The ester group can be hydrolyzed to the corresponding carboxylic acid or reduced to an alcohol, allowing further functionalization. Commonly employed in the preparation of heterocyclic compounds and bioactive molecules where a five-carbon spacer with a terminal reactive site is needed. Its tert-butyl ester group offers stability under various reaction conditions and can be deprotected under acidic conditions when required.

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