BOC-MENCH[CH3(CH2)2]-COOH
Boc-N-Me-Nva-OH
CAS: 136092-78-9
Molecular Formula: C11H21NO4
BOC-MENCH[CH3(CH2)2]-COOH - Names and Identifiers
BOC-MENCH[CH3(CH2)2]-COOH - Physico-chemical Properties
| Molecular Formula | C11H21NO4 |
| Molar Mass | 231.29 |
| Storage Condition | Store at RT. |
BOC-MENCH[CH3(CH2)2]-COOH - Risk and Safety
| Hazard Class | IRRITANT |
BOC-MENCH[CH3(CH2)2]-COOH - Introduction
Boc-N-Methyl-L-norvaline is an amino acid derivative with the following properties:
1. properties: Boc-N-methyl-L-norvaline is a solid, white to slightly yellow crystalline form. It is stable and soluble in some common organic solvents such as dimethyl sulfoxide and methylene chloride.
2. Uses: Boc-N-methyl-L-norvaline is mainly used as an amino acid protecting group in organic synthesis. It can be deprotected (Boc) to form the original amino acid, and then used in the synthesis of drugs, biological macromolecules and other organic compounds.
3. Preparation method: A common method for preparing Boc-N-methyl-L-norvaline is to react N-methyl-L-norvaline with Boc acid chloride. The reaction product can be purified by crystallization or column chromatography.
4. Safety Information: Boc-N-methyl-L-norvaline is generally relatively safe under normal conditions of use. However, because it is an organic compound, it is necessary to pay attention to protective measures, such as avoiding contact with eyes and skin, and avoiding inhalation or ingestion. When performing experimental operations, pay attention to safe operating procedures and wear appropriate protective equipment, such as gloves and safety glasses. During handling and storage, a well-ventilated environment and proper storage conditions should be maintained.
1. properties: Boc-N-methyl-L-norvaline is a solid, white to slightly yellow crystalline form. It is stable and soluble in some common organic solvents such as dimethyl sulfoxide and methylene chloride.
2. Uses: Boc-N-methyl-L-norvaline is mainly used as an amino acid protecting group in organic synthesis. It can be deprotected (Boc) to form the original amino acid, and then used in the synthesis of drugs, biological macromolecules and other organic compounds.
3. Preparation method: A common method for preparing Boc-N-methyl-L-norvaline is to react N-methyl-L-norvaline with Boc acid chloride. The reaction product can be purified by crystallization or column chromatography.
4. Safety Information: Boc-N-methyl-L-norvaline is generally relatively safe under normal conditions of use. However, because it is an organic compound, it is necessary to pay attention to protective measures, such as avoiding contact with eyes and skin, and avoiding inhalation or ingestion. When performing experimental operations, pay attention to safe operating procedures and wear appropriate protective equipment, such as gloves and safety glasses. During handling and storage, a well-ventilated environment and proper storage conditions should be maintained.
Last Update：2024-04-09 19:05:46
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Product Name: (S)-2-((tert-Butoxycarbonyl)(methyl)amino)pentanoicacid Request for quotationCAS: 136092-78-9
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View History
BOC-MENCH[CH3(CH2)2]-COOH
10349-57-2
29307-60-6
849924-48-7
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631-61-8
3550-35-4
1462249-75-7
pentachlorobenzonitrile
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10349-57-2
29307-60-6
849924-48-7
Benzotriazole sodium salt
631-61-8
3550-35-4
1462249-75-7
pentachlorobenzonitrile
Denka Silicon Nitride SN-F 2