2-[(tert-butoxycarbonyl)amino]benzoato
2-(boc-amino)benzoic acid
CAS: 68790-38-5
Molecular Formula: C12H15NO4
2-[(tert-butoxycarbonyl)amino]benzoato - Names and Identifiers
| Name | 2-(boc-amino)benzoic acid |
| Synonyms | BOC-ANT-OH Boc-2-Abz-OH BOC-ANTHRANILIC ACID BOC-AMINOBENZOIC ACID 2-(BOC-AMINO)BENZOIC ACID 2-(boc-amino)benzoic acid N-tert-Butoxycarbonylanthranilic acid 2-[(tert-butoxycarbonyl)amino]benzoato 2-(TERT-BUTYLOXYCARBONYLAMINO)-BENZOIC ACID |
| CAS | 68790-38-5 |
| InChI | InChI=1/C12H15NO4/c1-12(2,3)17-11(16)13-9-7-5-4-6-8(9)10(14)15/h4-7H,1-3H3,(H,13,16)(H,14,15) |
2-[(tert-butoxycarbonyl)amino]benzoato - Physico-chemical Properties
| Molecular Formula | C12H15NO4 |
| Molar Mass | 237.25 |
| Density | 1.242±0.06 g/cm3(Predicted) |
| Melting Point | 153-156°C (dec.) |
| Boling Point | 328.6±25.0 °C(Predicted) |
| Flash Point | 152.5°C |
| Vapor Presure | 7.58E-05mmHg at 25°C |
| BRN | 2848891 |
| pKa | 3.67±0.36(Predicted) |
| Storage Condition | Sealed in dry,2-8°C |
| Refractive Index | 1.574 |
2-[(tert-butoxycarbonyl)amino]benzoato - Risk and Safety
| Safety Description | S22 - Do not breathe dust. S24/25 - Avoid contact with skin and eyes. |
| WGK Germany | 3 |
| HS Code | 29242990 |
| Hazard Class | IRRITANT |
2-[(tert-butoxycarbonyl)amino]benzoato - Introduction
2-(boc-amino)benzoic acid, also known as 2-(boc-amino)benzoic acid or Boc-AA-PhCOOH, is an organic compound. The following is a description of its nature, use, preparation and safety information:
Nature:
-Appearance: White crystalline solid or powder
-Molecular formula: C13H17NO4
-Molecular weight: 251.28g/mol
-melting point: 163-166 ℃
-Solubility: Soluble in some organic solvents, such as dimethylformamide (DMF), dimethyl sulfoxide (DMSO), etc.
Use:
- 2-(boc-amino)benzoic acid is a commonly used protecting group reagent, which can be used to protect amino groups in organic synthesis.
-It can be used to synthesize peptides, amino acid derivatives and other pharmaceutical intermediates.
Preparation Method:
- 2-(boc-amino)benzoic acid can be obtained by reacting benzoic acid with an N-tert-butoxycarbonylamino compound (such as N-tert-butoxycarbonylcarbamate).
Safety Information:
- 2-(boc-amino) The specific safety information of benzoic acid may vary from supplier to supplier, so please check the relevant safety data sheet before use.
-Protective measures should be taken when touching, such as wearing gloves, protective glasses, wearing appropriate protective clothing, etc.
-When handling or using, take care to prevent inhalation of dust or solution, avoid skin contact and ingestion.
-In case of inadvertent contact or misuse, seek medical attention immediately or consult a professional doctor.
Nature:
-Appearance: White crystalline solid or powder
-Molecular formula: C13H17NO4
-Molecular weight: 251.28g/mol
-melting point: 163-166 ℃
-Solubility: Soluble in some organic solvents, such as dimethylformamide (DMF), dimethyl sulfoxide (DMSO), etc.
Use:
- 2-(boc-amino)benzoic acid is a commonly used protecting group reagent, which can be used to protect amino groups in organic synthesis.
-It can be used to synthesize peptides, amino acid derivatives and other pharmaceutical intermediates.
Preparation Method:
- 2-(boc-amino)benzoic acid can be obtained by reacting benzoic acid with an N-tert-butoxycarbonylamino compound (such as N-tert-butoxycarbonylcarbamate).
Safety Information:
- 2-(boc-amino) The specific safety information of benzoic acid may vary from supplier to supplier, so please check the relevant safety data sheet before use.
-Protective measures should be taken when touching, such as wearing gloves, protective glasses, wearing appropriate protective clothing, etc.
-When handling or using, take care to prevent inhalation of dust or solution, avoid skin contact and ingestion.
-In case of inadvertent contact or misuse, seek medical attention immediately or consult a professional doctor.
Last Update：2024-04-09 19:05:51
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