N-Boc-2-(4'-chlorophenyl)-DL-glycine - Names and Identifiers
Name | N-Boc-2-(4'-chlorophenyl)-DL-glycine
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Synonyms | N-Boc-RS-4-Chlorophenylglycine N-Boc-2-(4'-chlorophenyl)-DL-glycine N-BOC-2-(4'-CHLOROPHENYL)-DL-GLYCINE N-Boc-2-(4''-chlorophenyl)-DL-glycine N-Boc-amino-(4-chlorophenyl)acetic acid 4-Chloro-a-(Boc-aMino)-benzeneacetic acid tert-Butoxycarbonylamino(4-chlorophenyl)acetic acid tert-Butoxycarbonylamino(4-chlorophenyl)acetic acid [(tert-butoxycarbonyl)amino](4-chlorophenyl)acetic acid Benzeneacetic acid, 4-chloro-α-[[(1,1-dimethylethoxy)carbonyl]amino]- 2-(4-chlorophenyl)-2-[(2-methylpropan-2-yl)oxycarbonylamino]acetic acid
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CAS | 209525-73-5
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InChI | InChI=1/C13H16ClNO4/c1-13(2,3)19-12(18)15-10(11(16)17)8-4-6-9(14)7-5-8/h4-7,10H,1-3H3,(H,15,18)(H,16,17) |
N-Boc-2-(4'-chlorophenyl)-DL-glycine - Physico-chemical Properties
Molecular Formula | C13H16ClNO4
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Molar Mass | 285.72 |
Density | 1.272±0.06 g/cm3(Predicted) |
Boling Point | 438.8±40.0 °C(Predicted) |
Flash Point | 219.2°C |
Vapor Presure | 1.78E-08mmHg at 25°C |
pKa | 3.38±0.10(Predicted) |
Storage Condition | Sealed in dry,Room Temperature |
Refractive Index | 1.543 |
N-Boc-2-(4'-chlorophenyl)-DL-glycine - Introduction
N-Boc-2-(4 '-chlorophenyl)-DL-glycine is an organic compound also known as N-Boc-2-(4'-chlorophenyl)-DL-alanine. The following is a description of the properties, uses, preparation and safety information of the compound:
Nature:
N-Boc-2-(4 '-chroophenyl)-DL-glycine is a solid, white crystalline powder at room temperature. It is less soluble in water, but soluble in organic solvents such as methanol, dimethyl sulfoxide and methylene chloride.
Use:
N-Boc-2-(4 '-chlorophenyl)-DL-glycine is a common organic synthesis intermediate. It can be used to synthesize compounds such as drugs, bioactive molecules and functional materials. It is an important starting material for the synthesis of β-amino acids and biologically active organic molecules.
Method:
The preparation of N-Boc-2-(4 '-chroophenyl)-DL-glycine is generally accomplished by chemical synthetic methods. A common method is to obtain the product by reacting DL-glycine with 4-chlorobenzoic acid and a sulfuric acid dehydrating agent, followed by introduction of a protecting group (Boc protecting group).
Safety Information:
N-Boc-2-(4 '-DL-glycine)-is generally relatively safe under normal operating conditions, but any chemical needs to be operated under safe conditions. During use, avoid inhalation, contact with skin and eyes. Wear appropriate protective equipment, such as lab glasses, gloves and protective clothing. In addition, the compound should be stored in a dry, cool place and away from fire and flammable materials. When handling this compound, follow the relevant safety practices and recommendations.
Last Update:2024-04-09 20:52:54