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Home  > (S)-2-((tert-butoxycarbonyl)amino)-2-((1R,4S)-4-methylcyclohexyl)acetic acid

BA08209

1187224-06-1 | (S)-2-((tert-butoxycarbonyl)amino)-2-((1R,4S)-4-methylcyclohexyl)acetic acid

Packsize Purity Availability Price Discounted Price    Quantity
250mg 95% in stock $440.00 $308.00 -   +
1g 95% in stock $1,033.00 $723.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: BA08209
Chemical Name: (S)-2-((tert-butoxycarbonyl)amino)-2-((1R,4S)-4-methylcyclohexyl)acetic acid
CAS Number: 1187224-06-1
Molecular Formula: C14H25NO4
Molecular Weight: 271.3526
MDL Number: MFCD00007368
SMILES: C[C@@H]1CC[C@H](CC1)[C@@H](C(=O)O)NC(=O)OC(C)(C)C

 

Upstream Synthesis Route
  • The (S)-2-((tert-butoxycarbonyl)amino)-2-((1R,4S)-4-methylcyclohexyl)acetic acid, commonly referred to as $name$, is a versatile compound widely utilized in chemical synthesis processes. In particular, this compound serves as a crucial building block in the creation of various pharmaceutical agents and intricate organic molecules. Its unique structure and properties make it an essential component for the development of novel drugs, organic materials, and biologically active compounds. Furthermore, the (S)-2-((tert-butoxycarbonyl)amino)-2-((1R,4S)-4-methylcyclohexyl)acetic acid plays a vital role in the strategic design and synthesis of complex organic molecules with specific stereochemistry, enabling chemists to achieve precise control over the formation of chiral centers and asymmetric synthesis pathways. Its application in chemical synthesis extends to the creation of advanced materials, agrochemicals, and sophisticated intermediates required for various industries.
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