NALPHA-tert-Butoxycarbonyl-N-methyl-L-valine
boc-N-methyl-L-valine
CAS: 45170-31-8
Molecular Formula: C11H21NO4
NALPHA-tert-Butoxycarbonyl-N-methyl-L-valine - Names and Identifiers
| Name | boc-N-methyl-L-valine |
| Synonyms | Boc-N-me-Val Boc-N-Me-Val-OH Boc-L-N-Me-Val-OH BOC-N-METHYL-L-VAL-OH boc-N-methyl-L-valine N-(tert-butoxycarbonyl)-N-methyl-D-valine N-(tert-butoxycarbonyl)-N-methyl-L-valine N-[(tert-Butoxy)carbonyl]-N-methyl-L-valine NALPHA-tert-Butoxycarbonyl-N-methyl-L-valine N-alpha-t-butyloxycabonyl-N-alpha-Methyl-L-valine N-ALPHA-TERT-BUTYLOXYCABONYL-N-ALPHA-METHYL-L-VALINE (S)-2-((tert-Butoxycarbonyl)(Methyl)aMino)-3-Methylbutanoic acid |
| CAS | 45170-31-8 |
| InChI | InChI=1/C11H21NO4/c1-7(2)8(9(13)14)12(6)10(15)16-11(3,4)5/h7-8H,1-6H3,(H,13,14)/t8-/m1/s1 |
| InChIKey | XPUAXAVJMJDPDH-QMMMGPOBSA-N |
NALPHA-tert-Butoxycarbonyl-N-methyl-L-valine - Physico-chemical Properties
| Molecular Formula | C11H21NO4 |
| Molar Mass | 231.29 |
| Density | 1.069±0.06 g/cm3(Predicted) |
| Melting Point | 45-60°C |
| Boling Point | 322.4±21.0 °C(Predicted) |
| Specific Rotation(α) | -94 º (c=0.5% in ethanol) |
| Flash Point | 148.8°C |
| Solubility | Chloroform (Slightly), Ethanol (Slightly), Methanol (Slightly) |
| Vapor Presure | 5.74E-05mmHg at 25°C |
| Appearance | Solid |
| Color | Off-White |
| BRN | 2646180 |
| pKa | 4.03±0.10(Predicted) |
| Storage Condition | Keep in dark place,Sealed in dry,Room Temperature |
| Refractive Index | 1.466 |
| MDL | MFCD00038760 |
NALPHA-tert-Butoxycarbonyl-N-methyl-L-valine - Risk and Safety
| WGK Germany | 3 |
| HS Code | 29225090 |
| Hazard Class | IRRITANT |
NALPHA-tert-Butoxycarbonyl-N-methyl-L-valine - Introduction
boc-N-methyl-L-valine(boc-N-methyl-L-valine) is an organic compound. Its nature is white crystals, soluble in some organic solvents, such as dimethyl sulfoxide and dimethylformamide.
boc-N-methyl-L-valine are often used as raw materials and intermediates in the field of pharmaceutical synthesis and biochemistry. It can be used to synthesize polypeptides, proteins, and other biologically active molecules. As a protective group in the synthesis, Boc(t-butoxycarbonyl) can be removed by acid or base, making the synthesis process more convenient and efficient.
The preparation boc-N-methyl-L-valine generally adopts the method of chemical synthesis. In the synthesis, L-valine is first reacted with methylamine to produce N-methyl-L-valine, which is subsequently reacted with t-butoxycarbonyl chloroformate to give boc-N-methyl-L-valine.
Pay attention to the safety information of boc-N-methyl-L-valine when using or storing them. It is an organic compound that may be irritating to the respiratory tract, eyes and skin, and direct contact should be avoided. Wear protective glasses and gloves during operation, and ensure that the operating environment is well ventilated. In addition, this compound also need to pay attention to fire, moisture and away from oxidants, acids and alkaline substances.
boc-N-methyl-L-valine are often used as raw materials and intermediates in the field of pharmaceutical synthesis and biochemistry. It can be used to synthesize polypeptides, proteins, and other biologically active molecules. As a protective group in the synthesis, Boc(t-butoxycarbonyl) can be removed by acid or base, making the synthesis process more convenient and efficient.
The preparation boc-N-methyl-L-valine generally adopts the method of chemical synthesis. In the synthesis, L-valine is first reacted with methylamine to produce N-methyl-L-valine, which is subsequently reacted with t-butoxycarbonyl chloroformate to give boc-N-methyl-L-valine.
Pay attention to the safety information of boc-N-methyl-L-valine when using or storing them. It is an organic compound that may be irritating to the respiratory tract, eyes and skin, and direct contact should be avoided. Wear protective glasses and gloves during operation, and ensure that the operating environment is well ventilated. In addition, this compound also need to pay attention to fire, moisture and away from oxidants, acids and alkaline substances.
Last Update：2024-04-09 19:05:49
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CAS: 45170-31-8
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CAS: 45170-31-8
Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
QQ: 3008007409
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