(1S,2S)-2-Methylcyclopropane-1-carboxylicacid

97%

Reagent Code: #237817
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CAS Number 14590-52-4

science Other reagents with same CAS 14590-52-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 100.12 g/mol
Formula C₅H₈O₂
badge Registry Numbers
MDL Number MFCD19228287
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key chiral building block in the synthesis of active pharmaceutical ingredients, particularly in the production of pyrethroid insecticides and certain antiviral agents. Its rigid cyclopropane structure and defined stereochemistry make it valuable for introducing conformational restraint in drug design, enhancing selectivity and metabolic stability. Commonly employed in asymmetric synthesis to control stereochemical outcomes. Also utilized in the preparation of specialty agrochemicals where chirality impacts biological activity.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿7,440.00
250mg
10-20 days ฿12,240.00
1g
10-20 days ฿19,370.00
5g
10-20 days ฿52,420.00
(1S,2S)-2-Methylcyclopropane-1-carboxylicacid
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Used as a key chiral building block in the synthesis of active pharmaceutical ingredients, particularly in the production of pyrethroid insecticides and certain antiviral agents. Its rigid cyclopropane structure and defined stereochemistry make it valuable for introducing conformational restraint in drug design, enhancing selectivity and metabolic stability. Commonly employed in asymmetric synthesis to control stereochemical outcomes. Also utilized in the preparation of specialty agrochemicals where chir

Used as a key chiral building block in the synthesis of active pharmaceutical ingredients, particularly in the production of pyrethroid insecticides and certain antiviral agents. Its rigid cyclopropane structure and defined stereochemistry make it valuable for introducing conformational restraint in drug design, enhancing selectivity and metabolic stability. Commonly employed in asymmetric synthesis to control stereochemical outcomes. Also utilized in the preparation of specialty agrochemicals where chirality impacts biological activity.

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