(1R,3S)-3-(tert-Butoxycarbonylamino)cyclohexanecarboxylic Acid

97%

Reagent Code: #230297
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CAS Number 222530-39-4

science Other reagents with same CAS 222530-39-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 243.3 g/mol
Formula C₁₂H₂₁NO₄
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MDL Number MFCD04973107
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules requiring stereochemical control. Its protected amine and carboxylic acid functionalities make it valuable in peptide-like structure construction and in the preparation of cyclic analogs for drug discovery. Commonly employed in medicinal chemistry for designing enzyme inhibitors and receptor modulators due to its conformational rigidity and defined stereochemistry.

Available Sizes & Pricing

Size Availability Unit Price Quantity
200mg
10-20 days ฿671.00
5g
10-20 days ฿24,420.00
1g
10-20 days ฿5,080.00
(1R,3S)-3-(tert-Butoxycarbonylamino)cyclohexanecarboxylic Acid
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules requiring stereochemical control. Its protected amine and carboxylic acid functionalities make it valuable in peptide-like structure construction and in the preparation of cyclic analogs for drug discovery. Commonly employed in medicinal chemistry for designing enzyme inhibitors and receptor modulators due to its conformational rigidity and defined stereochemistry.

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules requiring stereochemical control. Its protected amine and carboxylic acid functionalities make it valuable in peptide-like structure construction and in the preparation of cyclic analogs for drug discovery. Commonly employed in medicinal chemistry for designing enzyme inhibitors and receptor modulators due to its conformational rigidity and defined stereochemistry.

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