(1R,3S)-3-Boc-Amino-cyclohexanecarboxylic acid

Product Name (1R,3S)-3-Boc-Amino-cyclohexanecarboxylic acid
CAT No. CS-DV-00052
CAS No. 222530-39-4
Category Impurities
Stock Enquire
Mol. Wt. Not Available
Mol. For. Not Available
Hazardous This is not a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Canonical Smiles CC(C)(C)OC(=O)NC1CCCC(C1)C(=O)O
InchIKey JSGHMGKJNZTKGF-BDAKNGLRSA-N
Inchl InChI=1S/C12H21NO4/c1-12(2,3)17-11(16)13-9-6-4-5-8(7-9)10(14)15/h8-9H,4-7H2,1-3H3,(H,13,16)(H,14,15)/t8-,9+/m1/s1
IUPAC (1R,3S)-3-[(2-methylpropan-2-yl)oxycarbonylamino]cyclohexane-1-carboxylic acid
Controlled No
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(1R,3S)-3-Boc-Amino-cyclohexanecarboxylic acid is a chemical compound that is commonly used in the field of organic chemistry. This compound is a derivative of cyclohexanecarboxylic acid and contains a Boc-protected amino group at the 3-position and a carboxylic acid group at the 1-position. The Boc-protecting group is used to prevent unwanted reactions from occurring at the amino group during chemical reactions. The (1R,3S)-stereochemistry of this compound refers to the relative orientation of the substituents on the cyclohexane ring. The stereochemistry is important because it affects the compound's reactivity and biological activity. This compound is often used as a building block in the synthesis of peptides and other bioactive molecules. It can be used to introduce the cyclohexane scaffold into a peptide sequence, which can alter the peptide's conformation and

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