CAS 144085-23-4
:BOC-(R)--ALLYL-PRO-OH
Description:
BOC-(R)-ALLYL-PRO-OH, with the CAS number 144085-23-4, is a chemical compound characterized by its structure, which includes a tert-butyloxycarbonyl (BOC) protecting group, an allyl group, and a proline derivative. This compound is typically used in organic synthesis, particularly in the field of peptide chemistry, where protecting groups are essential for selective reactions. The BOC group serves to protect the amine functionality of proline during synthesis, allowing for the selective modification of other reactive sites. The presence of the allyl group can facilitate further reactions, such as cross-coupling or addition reactions, making it a versatile intermediate. The compound is generally stable under standard laboratory conditions but may require specific handling procedures to maintain its integrity. Its solubility characteristics can vary depending on the solvent used, and it is important to consider its reactivity in the context of the desired synthetic pathway. Overall, BOC-(R)-ALLYL-PRO-OH is a valuable building block in the synthesis of more complex organic molecules.
Formula:C13H21NO4
InChI:InChI=1/C13H21NO4/c1-5-7-13(10(15)16)8-6-9-14(13)11(17)18-12(2,3)4/h5H,1,6-9H2,2-4H3,(H,15,16)/t13-/m0/s1
SMILES:C=CC[C@]1(CCCN1C(=O)OC(C)(C)C)C(=O)O
Synonyms:- Boc-(R)-Α-Allyl-Pro-Oh
- Boc-(R)-a-allylproline
- (R)-2-Allyl-1-Boc-2-pyrrolidinecarboxylic acid, Boc-α-allyl-L-proline
- 1-(tert-butoxycarbonyl)-2-prop-2-en-1-yl-L-proline
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Found 2 products.
(R)-2-Allyl-1-(Tert-Butoxycarbonyl)Pyrrolidine-2-Carboxylic Acid
CAS:Formula:C13H21NO4Purity:95%Color and Shape:SolidMolecular weight:255.3101

