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13734-40-2

boc-O-tert-butyl-L-threonine

CAS: 13734-40-2

Molecular Formula: C13H25NO5

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13734-40-2 - Names and Identifiers

Name boc-O-tert-butyl-L-threonine
Synonyms BOC-THR(BUT)-OH
Boc-Thr(tBu)-OH
Boc-Thr(But)-OH
BOC-L-THR(TBU)-OH
BOC-THREONINE(TBU)-OH
BOC-O-T-BUTYL-L-THREONINE
BOC-O-TERT-BUTYL-L-THREONINE
boc-O-tert-butyl-L-threonine
Boc-O-tert-butyl-L-threonine
N-T-boc-O-T-butyl-L-threonine
N-ALPHA-T-BOC-O-T-BUTYL-L-THREONINE
N-ALPHA-T-BUTOXYCARBONYL-O-T-BUTYL-L-THREONINE
N-(tert-butoxycarbonyl)-O-tert-butyl-L-threonine
N-ALPHA-TERT-BUTYLOXYCARBONYL-O-TERT-BUTYL-L-THREONINE
CAS 13734-40-2
InChI InChI=1/C13H25NO5/c1-8(18-12(2,3)4)9(10(15)16)14-11(17)19-13(5,6)7/h8-9H,1-7H3,(H,14,17)(H,15,16)/t8-,9+/m1/s1

13734-40-2 - Physico-chemical Properties

Molecular FormulaC13H25NO5
Molar Mass275.34
Density1.070±0.06 g/cm3(Predicted)
Melting Point95-98°C
Boling Point391.3±37.0 °C(Predicted)
Flash Point190.4°C
Solubility Soluble in DMF.
Vapor Presure3.27E-07mmHg at 25°C
AppearanceWhite powder or crystal
BRN4454820
pKa3.53±0.10(Predicted)
Storage Condition2-8°C
Refractive Index1.462
MDLMFCD00151115

13734-40-2 - Risk and Safety

WGK Germany3
HS Code2924 19 00

13734-40-2 - Introduction

N-tert-Butoxycarbonyl-O-tert-butyl-L-threonine, also known as N-Boc-O-tBu-L-serine, is an organic compound. Its molecular formula is C15H29NO6 and its structure contains the L-isomer of threonine.

N-tert-Butoxycarbonyl-O-tert-butyl-L-threonine is generally a white crystalline solid. It has good solubility, soluble in many organic solvents, such as methanol, ethanol, dimethylformamide and so on.

For the application of N-tert-butoxycarbonyl-O-tert-butyl-L-threonine, it is often used as a protecting group in organic synthesis. With the tert-butoxycarbonyl and tert-butyl protecting groups, the protected hydroxyl group can be protected during the synthesis to prevent further reactions. The use of protecting groups is very important in the synthesis of polypeptide or drug molecules.

The method for preparing N-tert-butoxycarbonyl-O-tert-butyl-L-threonine is generally obtained by reacting threonine with tert-butyryl chloride, and then reacting with tert-butyl sodium hydroxide to generate the target product. Specific procedures can refer to organic synthesis literature and laboratory manuals.
Last Update:2024-04-09 21:04:16
13734-40-2
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