3,5-DIMETHYLPYRROLE-2,4-DICARBOXYLIC ACID 4-ETHYL ESTER-2-T-BUTYL ESTER

98%

Reagent Code: #169953
label
Alias 3,5-dimethylpyrrole-2-carboxylic acid tert-butyl ester-4-carboxylic acid ethyl ester; sunitinib intermediate 1;1H-pyrrole-2,4-dicarboxylic acid, 3,5-dimethyl-, 2-(1,1-dimethylethyl) 4-ethyl ester
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CAS Number 86770-31-2

science Other reagents with same CAS 86770-31-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 267.32 g/mol
Formula C₁₄H₂₁NO₄
badge Registry Numbers
MDL Number MFCD02179394
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of heterocyclic compounds with biological activity. Its ester-protected structure allows selective reactions in multi-step organic syntheses, making it valuable in creating drug candidates targeting central nervous system disorders and inflammatory conditions. The compound’s pyrrole core with tailored substituents enhances binding affinity in medicinal chemistry applications. It is also employed in agrochemical research for designing novel pesticides and herbicides due to its ability to mimic bioactive natural products.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,100.00
inventory 5g
10-20 days ฿2,850.00
inventory 25g
10-20 days ฿8,450.00
inventory 100g
10-20 days ฿30,370.00

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3,5-DIMETHYLPYRROLE-2,4-DICARBOXYLIC ACID 4-ETHYL ESTER-2-T-BUTYL ESTER
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of heterocyclic compounds with biological activity. Its ester-protected structure allows selective reactions in multi-step organic syntheses, making it valuable in creating drug candidates targeting central nervous system disorders and inflammatory conditions. The compound’s pyrrole core with tailored substituents enhances binding affinity in medicinal chemistry applications. It is also employed in agrochemica

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of heterocyclic compounds with biological activity. Its ester-protected structure allows selective reactions in multi-step organic syntheses, making it valuable in creating drug candidates targeting central nervous system disorders and inflammatory conditions. The compound’s pyrrole core with tailored substituents enhances binding affinity in medicinal chemistry applications. It is also employed in agrochemical research for designing novel pesticides and herbicides due to its ability to mimic bioactive natural products.

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