(S)-2-Amino-3,3-dimethylbutanoic acid tert-butyl ester
H-TBU-GLY-OTBU HCL
CAS: 31556-74-8
Molecular Formula: C10H22ClNO2
(S)-2-Amino-3,3-dimethylbutanoic acid tert-butyl ester - Names and Identifiers
(S)-2-Amino-3,3-dimethylbutanoic acid tert-butyl ester - Physico-chemical Properties
| Molecular Formula | C10H22ClNO2 |
| Molar Mass | 223.74 |
| Density | 0.930±0.06 g/cm3(Predicted) |
| Boling Point | 87-89 °C(Press: 18 Torr) |
| pKa | 7.97±0.37(Predicted) |
| Storage Condition | Inert atmosphere,2-8°C |
(S)-2-Amino-3,3-dimethylbutanoic acid tert-butyl ester - Risk and Safety
| Hazard Symbols | Xn - Harmful |
| Risk Codes | R22 - Harmful if swallowed R51 - Toxic to aquatic organisms |
(S)-2-Amino-3,3-dimethylbutanoic acid tert-butyl ester - Upstream Downstream Industry
| Raw Materials | L-Valine, 3-methyl-N-[(phenylmethoxy)carbonyl]-, 1,1-dimethylethyl ester ISOPROPENYLMAGNESIUM BROMIDE Iodomethane tert-Butyl acetate L-tert-Leucine ISOBUTYLENE |
(S)-2-Amino-3,3-dimethylbutanoic acid tert-butyl ester - Introduction
H-TBU-GLY-OTBU HCL(H-TBU-GLY-OTBU HCL) is an organic compound. Its properties are as follows:
1. Appearance: white crystalline powder
2. Molecular formula: C12H25NO2 · HCl
3. Molecular weight: 253.79g/mol
4. Melting Point: 162-165 ℃
5. Solubility: insoluble in water, soluble in organic solvents such as ethanol and dimethylformamide.
H-TBU-GLY-OTBU HCL is commonly used in synthesis and research, it has the following main uses:
1. As a reagent for protecting amino acids: it can be used to protect the hydroxyl group of α-amino acids, thereby avoiding or reducing the interference of other functional groups.
2. Synthetic peptides and proteins: can be used to synthesize specific amino acids in peptide chains or protein sequences.
3. Biomedical research: It is commonly used in the study of protein structure and function, and studies its role in proteins by changing or protecting specific amino acid residues.
The method for preparing H-TBU-GLY-OTBU HCL is as follows:
1. First, tert-butyl methylimidoyl chloride is reacted with glycine to obtain tert-butyl glycine.
2. Glycine tert-butyl ester is then reacted with sodium tert-butyl azide to form glycine tert-butyl ester with the temporary protecting group being tert-butoxycarbonyl.
3. Finally, tert-butanol and hydrochloric acid were added to the reaction system to obtain H-TBU-GLY-OTBU HCL.
For safety information, please observe the following precautions:
1. H-TBU-GLY-OTBU HCL should avoid direct contact with skin, eyes and mucous membranes to avoid irritation or injury.
2. In the operation, should wear appropriate personal protective equipment, such as gloves, goggles, etc.
3. When storing and handling the compound, keep the room in a dry and well ventilated environment.
4. H-TBU-GLY-OTBU HCL should be properly stored to avoid exposure to heat sources and open flames to avoid fire.
5. Please strictly abide by the rules and regulations for the storage and disposal of chemicals, and pay attention to prevent the leakage and discharge of chemicals to ensure the safety of individuals and the environment.
1. Appearance: white crystalline powder
2. Molecular formula: C12H25NO2 · HCl
3. Molecular weight: 253.79g/mol
4. Melting Point: 162-165 ℃
5. Solubility: insoluble in water, soluble in organic solvents such as ethanol and dimethylformamide.
H-TBU-GLY-OTBU HCL is commonly used in synthesis and research, it has the following main uses:
1. As a reagent for protecting amino acids: it can be used to protect the hydroxyl group of α-amino acids, thereby avoiding or reducing the interference of other functional groups.
2. Synthetic peptides and proteins: can be used to synthesize specific amino acids in peptide chains or protein sequences.
3. Biomedical research: It is commonly used in the study of protein structure and function, and studies its role in proteins by changing or protecting specific amino acid residues.
The method for preparing H-TBU-GLY-OTBU HCL is as follows:
1. First, tert-butyl methylimidoyl chloride is reacted with glycine to obtain tert-butyl glycine.
2. Glycine tert-butyl ester is then reacted with sodium tert-butyl azide to form glycine tert-butyl ester with the temporary protecting group being tert-butoxycarbonyl.
3. Finally, tert-butanol and hydrochloric acid were added to the reaction system to obtain H-TBU-GLY-OTBU HCL.
For safety information, please observe the following precautions:
1. H-TBU-GLY-OTBU HCL should avoid direct contact with skin, eyes and mucous membranes to avoid irritation or injury.
2. In the operation, should wear appropriate personal protective equipment, such as gloves, goggles, etc.
3. When storing and handling the compound, keep the room in a dry and well ventilated environment.
4. H-TBU-GLY-OTBU HCL should be properly stored to avoid exposure to heat sources and open flames to avoid fire.
5. Please strictly abide by the rules and regulations for the storage and disposal of chemicals, and pay attention to prevent the leakage and discharge of chemicals to ensure the safety of individuals and the environment.
Last Update：2024-04-10 22:29:15
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CAS: 31556-74-8
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Product Name: H-TBU-GLY-OTBU HCL Visit Supplier Webpage Request for quotation
CAS: 31556-74-8
Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
QQ: 3008007409
Wechat: 18301782025
CAS: 31556-74-8
Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
QQ: 3008007409
Wechat: 18301782025
View History
Raw Materials for (S)-2-Amino-3,3-dimethylbutanoic acid tert-butyl ester
L-Valine, 3-methyl-N-[(phenylmethoxy)carbonyl]-, 1,1-dimethylethyl ester
ISOPROPENYLMAGNESIUM BROMIDE
Iodomethane
tert-Butyl acetate
L-tert-Leucine
ISOBUTYLENE
ISOPROPENYLMAGNESIUM BROMIDE
Iodomethane
tert-Butyl acetate
L-tert-Leucine
ISOBUTYLENE