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142910-85-8

(2-Amino-1-Phenyl-Ethyl)-Carbamic Acid Tert-Butyl Ester

CAS: 142910-85-8

Molecular Formula: C13H20N2O2

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142910-85-8 - Names and Identifiers

Name (2-Amino-1-Phenyl-Ethyl)-Carbamic Acid Tert-Butyl Ester
Synonyms α-(Boc-aMino)phenethylaMine
alpha-(Boc-amino)phenethylamine
2-(Boc-amino)-2-phenylethylamine
tert-Butyl (2-amino-1-phenylethyl)carbamate
tert-Butyl N-(2-amino-1-phenylethyl)carbamate
1,1-Dimethylethyl (2-amino-1-phenylethyl)carbamate
2-Methyl-2-propanyl-(2-amino-1-phenylethyl)carbamat
2-Methyl-2-propanyl (2-amino-1-phenylethyl)carbamate
(2-Amino-1-Phenyl-Ethyl)-Carbamic Acid Tert-Butyl Ester
(2-AMINO-1-PHENYL-ETHYL)-CARBAMIC ACID TERT-BUTYL ESTER
CarbaMic acid, N-(2-aMino-1-phenylethyl)-, 1,1-diMethylethyl ester
Carbamic acid, N-(2-amino-1-phenylethyl)-, 1,1-dimethylethyl ester
CAS 142910-85-8
InChI InChI=1/C13H20N2O2/c1-13(2,3)17-12(16)15-11(9-14)10-7-5-4-6-8-10/h4-8,11H,9,14H2,1-3H3,(H,15,16)

142910-85-8 - Physico-chemical Properties

Molecular FormulaC13H20N2O2
Molar Mass236.31
Density1.066±0.06 g/cm3(Predicted)
Melting Point85-90°C
Boling Point372.2±35.0 °C(Predicted)
Flash Point178.903°C
Vapor Presure0mmHg at 25°C
pKa11?+-.0.46(Predicted)
Storage Condition2-8°C(protect from light)
Refractive Index1.524
MDLMFCD09027881

142910-85-8 - Risk and Safety

Hazard SymbolsXn - Harmful
Harmful
Risk CodesR22 - Harmful if swallowed
R37/38 - Irritating to respiratory system and skin.
R41 - Risk of serious damage to eyes
Safety DescriptionS26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S39 - Wear eye / face protection.
WGK Germany3

142910-85-8 - Introduction

tert-Butyl N-(2-amino-1-phenylethyl) carbamate, often abbreviated as Boc-β-alanine, is an organic compound. The following is a description of its nature, use, formulation and safety information:

Nature:
-Appearance: Colorless or white crystalline powder
-Molecular formula: C14H22N2O4
-Molecular weight: 286.34g/mol
-Melting point: 89-92 ℃
-Soluble: Soluble in ethanol, ether and dimethyl sulfoxide

Use:
- Boc-β-alanine is commonly used as a protecting group in organic synthesis to protect the amino functional group of compounds such as amino acids and peptides.
-It can also be used as a pharmaceutical intermediate for the synthesis of biologically active compounds.
-In addition, Boc-β-alanine can also be used in the fields of protein engineering and peptide synthesis.

Preparation Method:
The preparation of Boc-β-alanine typically involves the following steps:
1. Condensation reaction of 2-amino-1-phenylethanol and tert-butyl formate to obtain N-(2-amino-1-phenylethyl) carbamic acid;
2. Ethylating the resulting product to obtain the final product Boc-β-alanine.

Safety Information:
- Boc-β-alanine is considered safe under routine experimental conditions.
-But it may be irritating to the skin and eyes, so appropriate protective measures should be taken when handling it.
-Avoid contact with oxidants and acids during use and storage.

Please note that for the specific use and preparation conditions of chemical substances, you should also carefully refer to relevant literature and experimental methods.
Last Update:2024-04-09 20:52:54
142910-85-8
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SHANGHAI ACMEC BIOCHEMICAL TECHNOLOGY CO., LTD.
Spot supply
Product Name: 2-(Boc-amino)-2-phenylethylamine Visit Supplier Webpage Request for quotation
CAS: 142910-85-8
Tel: +86-400-900-4166
Email: product@acmec-e.com
Mobile: +86-18621343501
QQ: 2881950922 Click to send a QQ message
Wechat: 18621343501
WhatsApp: +86-18621343501
Shanghai Macklin Biochemical Co., Ltd
Spot supply
Product Name: 2-(Boc-amino)-2-phenylethylamine Visit Supplier Webpage Request for quotation
CAS: 142910-85-8
Tel: +86-18821248368
Email: Int06@meryer.com
Mobile: +86-18821248368
QQ: 495145328 Click to send a QQ message
WhatsApp: +86-18821248368
Shanghai Yuanye Bio-Technology Co., Ltd.
Product Name: 2-(Boc-amino)-2-phenylethylamine Visit Supplier Webpage Request for quotation
CAS: 142910-85-8
Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
QQ: 3008007409 Click to send a QQ message
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