tert-butyl (1S)-2-amino-1-methyl-2-oxoethylcarbamate
Boc-L-alanine amide
CAS: 85642-13-3
Molecular Formula: C8H16N2O3
tert-butyl (1S)-2-amino-1-methyl-2-oxoethylcarbamate - Names and Identifiers
| Name | Boc-L-alanine amide |
| Synonyms | Boc-Ala-NH2 BOC-ALA-NH2 BOC-L-ALA-NH2 BOC-Beta-ala-NH2 Boc-L-alanine amide N-t-Butyloxycarbonyl-L-alanine amide N-tert-Butoxycarbonyl-L-alanine amide N-tert-Butoxycarbonyl-L-alanine amide N~2~-(tert-butoxycarbonyl)-L-alaninamide N-alpha-t-Butyloxycarbonyl-beta-alanine amide tert-butyl (1S)-2-amino-1-methyl-2-oxoethylcarbamate |
| CAS | 85642-13-3 |
| EINECS | 1533716-785-6 |
| InChI | InChI=1/C8H16N2O3/c1-5(6(9)11)10-7(12)13-8(2,3)4/h5H,1-4H3,(H2,9,11)(H,10,12)/t5-/m0/s1 |
tert-butyl (1S)-2-amino-1-methyl-2-oxoethylcarbamate - Physico-chemical Properties
| Molecular Formula | C8H16N2O3 |
| Molar Mass | 188.22 |
| Density | 1.081±0.06 g/cm3(Predicted) |
| Melting Point | 124-125 °C |
| Boling Point | 343.1±25.0 °C(Predicted) |
| Flash Point | 161.3°C |
| Water Solubility | Soluble in water or 1% acetic acid. |
| Vapor Presure | 7.19E-05mmHg at 25°C |
| Appearance | Solid |
| pKa | 11.38±0.46(Predicted) |
| Storage Condition | Sealed in dry,Room Temperature |
| Refractive Index | 1.463 |
tert-butyl (1S)-2-amino-1-methyl-2-oxoethylcarbamate - Introduction
Boc-L-alanine amide is an organic compound with the chemical formula C9H18N2O3. It is an L-alaninamide with a protecting group (Boc group, t-butoxycarbonyl group) in the structure.
Boc-L-alanine is commonly used as an amino acid protection reagent in organic synthesis. The protecting group (Boc group) can protect the amine group from reacting with other reagents during the synthesis, thereby selectively reacting other functional groups. It is commonly used in the synthesis of polypeptide or protein sequences having an L-alanine amine group. At the same time, Boc-L-alanine can also be used as an intermediate in drug development.
Boc-L-alanine is generally prepared by adding dimethyl carbonate to a mixture of Boc-L-alanine amide hydrochloride and sodium bicarbonate. The reaction needs to be carried out in a dry environment.
For safety information, Boc-L-alanine amide is dangerous. It can pose potential risks to health and the environment. When using, you need to pay attention to protective measures, such as wearing chemical protective gloves and eye protection. In addition, the compound should be stored and handled properly, avoiding exposure to high temperatures, fire and oxidizing agents.
Boc-L-alanine is commonly used as an amino acid protection reagent in organic synthesis. The protecting group (Boc group) can protect the amine group from reacting with other reagents during the synthesis, thereby selectively reacting other functional groups. It is commonly used in the synthesis of polypeptide or protein sequences having an L-alanine amine group. At the same time, Boc-L-alanine can also be used as an intermediate in drug development.
Boc-L-alanine is generally prepared by adding dimethyl carbonate to a mixture of Boc-L-alanine amide hydrochloride and sodium bicarbonate. The reaction needs to be carried out in a dry environment.
For safety information, Boc-L-alanine amide is dangerous. It can pose potential risks to health and the environment. When using, you need to pay attention to protective measures, such as wearing chemical protective gloves and eye protection. In addition, the compound should be stored and handled properly, avoiding exposure to high temperatures, fire and oxidizing agents.
Last Update：2024-04-09 20:52:54
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Spot supply
Product Name: Boc-Ala-NH2 Visit Supplier Webpage Request for quotationCAS: 85642-13-3
Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
QQ: 3008007409
Wechat: 18301782025
Multiple Specifications
Product Name: Boc-Ala-NH2 Request for quotationCAS: 85642-13-3
Tel: 86-10-10086 81625225
Email: yeqim@boyechemicals.com
Mobile: 86-15387090420
QQ: 1377812380
Wechat: 15387090420
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