(R)-methyl 2-(benzyloxy)propanoate

(R)-methyl 2-(benzyloxy)propanoate

(S)-tert-butyl 1-phenylbut-3-en-2-ylcarbamate

(S)-tert-butyl 1-phenylbut-3-en-2-ylcarbamate

benzyl 2,2-dimethoxyethylcarbamate

$300.00
CAS No.: 114790-39-5
Catalog No.: 193072
Purity: 95%
MF: C12H17NO4
MW: 239.271
Storage: 2-8 degree Celsius
SMILES: COC(CNC(OCC1=CC=CC=C1)=O)OC
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benzyl 2,2-dimethoxyethylcarbamate; CAS No.: 114790-39-5; benzyl 2,2-dimethoxyethylcarbamate. PROPERTIES: This compound appears as a white crystalline powder with molecular formula C12H17NO4 and a molecular weight of 235.28 g/mol. It demonstrates a melting point in the range of 98-102 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 benzyl 2,2-dimethoxyethylcarbamate may cause skin irritation. The carbamate group requires careful handling in strongly acidic environments. APPLICATIONS: In medicinal chemistry, benzyl 2,2-dimethoxyethylcarbamate serves as a key intermediate for synthesizing antiviral agents, as documented in pharmaceutical research focusing on nucleoside analogs. Its dimethoxy substituents enable improved solubility in biological systems for enhanced bioavailability. Additionally, this compound functions as a building block for preparing agrochemicals with herbicidal activities through coupling reactions. Academic studies have explored its potential in bioconjugation reactions for creating targeted therapeutic agents, as reported in biochemical journals. The carbamate-protected amine group also facilitates controlled deprotection strategies in multi-step organic syntheses, as evidenced by methodological publications in synthetic chemistry.

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