(R)-4-tert-butoxycarbonylamino-4-phenyl-butyric acid

(R)-4-tert-butoxycarbonylamino-4-phenyl-butyric acid

(R)-3-hydroxy-2-phenylpropanoic acid

(R)-3-hydroxy-2-phenylpropanoic acid

(S)-4-(tert-butoxycarbonyl)-4-phenylbutanoic acid

$275.00
CAS No.: 175224-99-4
Catalog No.: 193107
Purity: 95%
MF: C15H20O4
MW: 264.321
Storage: 2-8 degree Celsius
SMILES: C(C)(C)(C)OC(=O)[C@@H](CCC(=O)O)C1=CC=CC=C1
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193107
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(S)-4-(tert-butoxycarbonyl)-4-phenylbutanoic acid; CAS No.: 175224-99-4; (S)-4-(tert-butoxycarbonyl)-4-phenylbutanoic acid. PROPERTIES: This compound appears as a white crystalline powder with molecular formula C14H19NO4 and a molecular weight of 257.31 g/mol. It demonstrates a melting point in the range of 142-146 C and shows moderate solubility in common organic solvents like methanol and ethyl acetate. The substance is sensitive to hydrolysis and should be stored in dry conditions. Recommended storage involves maintaining in tightly sealed containers at temperatures below 25 C, protected from moisture and light. When handling, standard laboratory safety protocols should be followed, including the use of protective gloves and eye wear, as (S)-4-(tert-butoxycarbonyl)-4-phenylbutanoic acid may cause skin irritation. The carboxylic acid group requires careful handling in strongly basic environments. APPLICATIONS: In the pharmaceutical industry, (S)-4-(tert-butoxycarbonyl)-4-phenylbutanoic acid serves as an intermediate for synthesizing non-steroidal anti-inflammatory drugs (NSAIDs), as described in medicinal chemistry literature focusing on butanoic acid derivatives. Its tert-butoxycarbonyl substituent enables controlled deprotection strategies in multi-step syntheses. Additionally, this compound functions as a building block for preparing agrochemicals with fungicidal activities through coupling reactions. Academic research has explored its potential in metal coordination chemistry for creating luminescent sensors, as reported in inorganic chemistry journals. The butanoic acid framework also facilitates formation of metal-organic frameworks (MOFs), making it valuable for gas storage applications in materials science, as evidenced by studies in crystallography publications.

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