undecyl 6-bromohexanoate

98%

Reagent Code: #244964
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CAS Number 959040-06-3

science Other reagents with same CAS 959040-06-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 349.35 g/mol
Formula C₁₇H₃₃BrO₂
badge Registry Numbers
MDL Number MFCD34178803
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used primarily as an intermediate in organic synthesis, this compound serves in the preparation of specialty polymers and functionalized long-chain molecules. Its bromine functionality allows for further chemical modifications, such as nucleophilic substitution or coupling reactions, enabling the introduction of the ester-linked alkyl chain into more complex structures. It finds application in research settings for developing surfactants, lubricants, and bioactive molecule analogs. The spacer group provided by the bromohexanoate moiety is useful in constructing molecules with tailored hydrophobic and reactive characteristics.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,960.00
inventory 250mg
10-20 days ฿6,630.00
inventory 5g
10-20 days ฿53,000.00
inventory 1g
10-20 days ฿17,640.00

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undecyl 6-bromohexanoate
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Used primarily as an intermediate in organic synthesis, this compound serves in the preparation of specialty polymers and functionalized long-chain molecules. Its bromine functionality allows for further chemical modifications, such as nucleophilic substitution or coupling reactions, enabling the introduction of the ester-linked alkyl chain into more complex structures. It finds application in research settings for developing surfactants, lubricants, and bioactive molecule analogs. The spacer group provi

Used primarily as an intermediate in organic synthesis, this compound serves in the preparation of specialty polymers and functionalized long-chain molecules. Its bromine functionality allows for further chemical modifications, such as nucleophilic substitution or coupling reactions, enabling the introduction of the ester-linked alkyl chain into more complex structures. It finds application in research settings for developing surfactants, lubricants, and bioactive molecule analogs. The spacer group provided by the bromohexanoate moiety is useful in constructing molecules with tailored hydrophobic and reactive characteristics.

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