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AB45673

109183-71-3 | Boc-L-cyclohexylglycine

Packsize Purity Availability Price Discounted Price    Quantity
250mg 97% in stock $6.00 $4.00 -   +
1g 97% in stock $7.00 $5.00 -   +
5g 97% in stock $9.00 $6.00 -   +
10g 97% in stock $12.00 $9.00 -   +
25g >97% in stock $19.00 $13.00 -   +
100g 97% in stock $62.00 $44.00 -   +
500g 97% in stock $307.00 $215.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AB45673
Chemical Name: Boc-L-cyclohexylglycine
CAS Number: 109183-71-3
Molecular Formula: C13H23NO4
Molecular Weight: 257.3260
MDL Number: MFCD02684452
SMILES: O=C(OC(C)(C)C)N[C@@H](C1CCCCC1)C(=O)O

 

Computed Properties
Complexity: 303  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 1  
Heavy Atom Count: 18  
Hydrogen Bond Acceptor Count: 4  
Hydrogen Bond Donor Count: 2  
Rotatable Bond Count: 5  
XLogP3: 2.9  

 

 

Upstream Synthesis Route
  • N-Boc-L-cyclohexylglycine is a versatile chemical compound widely used in organic synthesis. Due to the presence of the Boc (tert-butoxycarbonyl) protecting group, this amino acid derivative serves as a valuable building block in peptide chemistry. When incorporated into peptide synthesis, N-Boc-L-cyclohexylglycine can efficiently protect the amino group of the adjacent amino acid residue, allowing for selective manipulation of the peptide sequence.Moreover, this compound finds application in the preparation of various pharmaceuticals and bioactive molecules. Its unique structure and reactivity make it a valuable tool for chemists in the design and synthesis of complex organic molecules. Additionally, N-Boc-L-cyclohexylglycine can be utilized as a chiral auxiliary in asymmetric synthesis to control the stereochemistry of reactions, further expanding its utility in chemical transformations.Overall, N-Boc-L-cyclohexylglycine plays a crucial role in modern chemical synthesis, enabling the creation of diverse compounds with specific functionalities and stereochemistries. Its versatility and compatibility with various reaction conditions make it an essential component in the toolkit of synthetic chemists.
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