N-[[(1,1-DiMethylethyl)aMino]carbonyl]-3-Methyl-L-valine - Names and Identifiers
Name | (2S)-2-(tert-butylcarbamoylamino)-3,3-dimethyl-butanoic acid
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Synonyms | Boceprevir INT 2 Boceprevir Intermediate 4 N-tert-Butylcarbamoyl-L-tert-leucine N-tert-ButylcarbaMoyl-L-tert-leucine N-(tert-Butylcarbamoyl)-3-methyl-L-valine (S)-2-(3-tert-Butylureido)-3,3-dimethylbutanoic acid (S)-2-(3-tert-butylureido)-3,3-diMethylbutanoic acid [ N-[[(1,1-DiMethylethyl)aMino]carbonyl]-3-Methyl-L-valine L-Valine,N-[[(1,1-diMethylethyl)aMino]carbonyl]-3-Methyl- L-valine, N-[[(1,1-dimethylethyl)amino]carbonyl]-3-methyl- (2S)-2-(tert-butylcarbaMoylaMino)-3,3-diMethyl-butanoic acid (2S)-2-(tert-butylcarbamoylamino)-3,3-dimethyl-butanoic acid (2S)-2-(tert-ButylaMinocarbonylaMino)-3,3-diMethylbutanoic Acid
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CAS | 101968-85-8
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EINECS | 600-257-4 |
InChI | InChI=1/C11H22N2O3/c1-10(2,3)7(8(14)15)12-9(16)13-11(4,5)6/h7H,1-6H3,(H,14,15)(H2,12,13,16)/t7-/m1/s1 |
N-[[(1,1-DiMethylethyl)aMino]carbonyl]-3-Methyl-L-valine - Physico-chemical Properties
Molecular Formula | C11H22N2O3
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Molar Mass | 230.3 |
Density | 1.047 |
Melting Point | 182 °C(dec.) |
Boling Point | 407.6±28.0 °C(Predicted) |
Flash Point | 200.3°C |
Solubility | Methanol |
Vapor Presure | 8.74E-08mmHg at 25°C |
Appearance | White solid |
Color | White |
pKa | 4.28±0.10(Predicted) |
Storage Condition | Sealed in dry,Room Temperature |
Refractive Index | 1.472 |
MDL | MFCD12796012 |
N-[[(1,1-DiMethylethyl)aMino]carbonyl]-3-Methyl-L-valine - Introduction
N-tert-Butylaminocarbonyl-3-methyl-L-valine is a chemical compound with the following properties:
1. nature: it is a white crystalline solid, stable at room temperature. It is an amino acid derivative with certain solubility, soluble in some organic solvents such as methanol and ether.
2. use: N-tert-butyl amino carbonyl -3-methyl-L-valine is mainly used in the field of medicine and biochemistry. It can be used as an intermediate in the synthesis of drugs for the synthesis of biologically active target compounds. In addition, it can be used as a tool to study protein structure and function.
3. Production Method: The synthesis of N-tert-butyroaminocarbon-3-methyl-L-valine is usually carried out by a multi-step reaction. A common preparation method is to use L-valine as a raw material, add a tert-butoxycarbonyl (BOC) protecting group under suitable conditions, and then perform a methylation reaction.
4. Safety information: For the safety of this compound, the following points need to be paid attention to: First, it may have an irritating effect on the eyes, skin and respiratory tract, so it is necessary to avoid contact and inhalation during operation. Second, in the handling and storage should pay attention to avoid contact with oxidants, acids and other substances, to avoid dangerous reactions. Finally, the waste of chemical compounds should be properly managed to avoid pollution to the environment. When using this compound in any chemical laboratory or industrial production environment, it should be strictly handled in accordance with safe operating practices.
Last Update:2024-04-09 21:00:56