Home Chemistry Organic Building Blocks Amides Tert-Butyl (1-Phenylethyl)Carbamate
These compounds have the same murcko framework: benzene,and at least 1 kind of functional groups( —CH(CH3)NHCOOC(CH3)3).
Hydrolysis: Treatment with acid or base can lead to hydrolysis of the carbamate group, resulting in the formation of tert-butylamine and phenylacetic acid or its salts. Reaction with Acid: C(CH3)3-C6H5-CH(NHCOOC(CH3)3)2 + HCl → C(CH3)3-C6H5-CH(NH2)2 + HCOOC(CH3)3 + Cl-; Reaction with Base: C(CH3)3-C6H5-CH(NHCOOC(CH3)3)2 + NaOH → C(CH3)3-C6H5-CH(NH2)2 + HCOOC(CH3)3 + Na+
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Methyl (S)-3-(1-((tert-butoxycarbonyl)amino)ethyl)benzoate
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4-(1-((tert-Butoxycarbonyl)amino)ethyl)benzoic acid
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(R)-3-(1-((tert-Butoxycarbonyl)amino)ethyl)benzoic acid
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(S)-3-(1-((tert-Butoxycarbonyl)amino)ethyl)benzoic acid
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(R)-tert-Butyl (1-(3-bromophenyl)ethyl)carbamate
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(R)-tert-Butyl (1-(4-bromophenyl)ethyl)carbamate
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(S)-tert-Butyl (1-(4-bromophenyl)ethyl)carbamate
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(S)-tert-Butyl (1-(2-bromophenyl)ethyl)carbamate
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tert-Butyl (S)-(1-(3-aminophenyl)ethyl)carbamate
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tert-Butyl (1-(4-bromophenyl)ethyl)carbamate
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tert-Butyl (1-(3-bromophenyl)ethyl)carbamate
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(R)-tert-Butyl (1-(2-nitrophenyl)ethyl)carbamate
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tert-Butyl (1-(2-bromophenyl)ethyl)carbamate
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Methyl 3-(1-((tert-butoxycarbonyl)amino)ethyl)benzoate
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3-(1-((tert-Butoxycarbonyl)amino)ethyl)benzoic acid
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(R)-tert-Butyl (1-(2-bromophenyl)ethyl)carbamate
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tert-Butyl (1-(3-(hydroxymethyl)phenyl)ethyl)carbamate
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