(S)-Benzyl tert-butyl (3,3-dimethylbutane-1,2-diyl)dicarbamate

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(R)-2-Hydroxy-2-(4-hydroxyphenyl)acetic acid

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Benzyl (2,2-dimethoxyethyl)(methyl)carbamate

$180.00
CAS No.: 1355573-66-8
Catalog No.: 193088
Purity: 95%
MF: C13H19NO4
MW: 253.298
Storage: 2-8 degree Celsius
SMILES: COC(CN(C(OCC1=CC=CC=C1)=O)C)OC
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193088
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Benzyl (2,2-dimethoxyethyl)(methyl)carbamate; CAS No.: 1355573-66-8; Benzyl (2,2-dimethoxyethyl)(methyl)carbamate. 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-dimethoxyethyl)(methyl)carbamate may cause skin irritation. The carbamate group requires careful handling in strongly acidic environments. APPLICATIONS: In the pharmaceutical industry, Benzyl (2,2-dimethoxyethyl)(methyl)carbamate serves as an intermediate for synthesizing non-steroidal anti-inflammatory drugs (NSAIDs), as described in medicinal chemistry literature focusing on carbamate derivatives. Its dimethoxyethyl substituent enables improved solubility in biological systems for enhanced bioavailability. Additionally, this compound functions as a building block for preparing agrochemicals with fungicidal activities through formation of urea derivatives. Academic research has explored its potential in asymmetric catalysis for enantioselective synthesis, as reported in organic chemistry 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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