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(S)-4-(叔丁氧基)-3-((叔丁氧基羰基)氨基)-4-氧代丁酸

Boc-Asp-OtBu

CAS: 34582-32-6

Molecular Formula: C13H23NO6

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(S)-4-(叔丁氧基)-3-((叔丁氧基羰基)氨基)-4-氧代丁酸 - Names and Identifiers

Name Boc-Asp-OtBu
Synonyms Boc-Asp-OtBu
5-BOC-Asp-Ot Bu
Boc-Asp-OtBu . DCHA
Boc-L-aspartic acid 1-tert-butyl ester
N-tert-Butoxycarbonyl-L-aspartic acid 1-tert-butyl ester
N-(tert-Butoxycarbonyl)-L-aspartic acid α-tert butyl ester
N-(tert-Butoxycarbonyl)-L-aspartic acid 1-tert-butyl ester
(2S)-2-(tert-Butoxycarbonylamino)succinic acid 1-tert-butyl ester
N-[[(tert-Butyl)oxy]carbonyl]-L-aspartic acid 4-(tert-butyl) ester
L-Asparticacid, N-[(1,1-diMethylethoxy)carbonyl]-, 1-(1,1-diMethylethyl) ester
(3S)-4-tert-butoxy-3-[(tert-butoxycarbonyl)amino]-4-oxobutanoic acid (non-preferred name)
(3s)-4-[(2-Methylpropan-2-yl)oxy]-3-[(2-Methylpropan-2-yl)oxycarbonylaMino]-4-oxobutanoic Acid
CAS 34582-32-6
EINECS 1592732-453-0
InChI InChI=1/C13H23NO6/c1-12(2,3)19-10(17)8(7-9(15)16)14-11(18)20-13(4,5)6/h8H,7H2,1-6H3,(H,14,18)(H,15,16)/t8-/m0/s1

(S)-4-(叔丁氧基)-3-((叔丁氧基羰基)氨基)-4-氧代丁酸 - Physico-chemical Properties

Molecular FormulaC13H23NO6
Molar Mass289.32
Density1.139
Melting Point101-103?C
Boling Point429.0±40.0 °C(Predicted)
Flash Point213.3°C
Solubility DMSO (Slightly), Methanol (Slightly)
Vapor Presure1.46E-08mmHg at 25°C
AppearancePowder
ColorWhite
BRN4191701
pKa4.13±0.19(Predicted)
Storage ConditionSealed in dry,2-8°C
Refractive Index1.47

(S)-4-(叔丁氧基)-3-((叔丁氧基羰基)氨基)-4-氧代丁酸 - Risk and Safety

WGK Germany3
HS Code2924 19 00

(S)-4-(叔丁氧基)-3-((叔丁氧基羰基)氨基)-4-氧代丁酸 - Introduction

Boc-Asp-OtBu, commonly known as Boc-Asp-OtBu, is an organic compound. The following is an introduction to some of its properties, uses, formulation and safety information:

Nature:
-Appearance: Colorless crystalline or powdery objects.
-Molecular formula: C≡H≡NO-7.
-Molecular weight: 393.47g/mol.
-Melting point: about 68-70°C.
-Solubility: Soluble in some organic solvents, such as dimethylformamide (DMF) and dichloromethane (DCM).

Use:
- Boc-Asp-OtBu is a commonly used protecting group, often used in the synthesis of peptides and protein compounds. It can protect the carboxyl and amino groups of glutamic acid (Asp) and prevent accidental reactions and degradation.
- Boc-Asp-OtBu can also be used as reaction intermediates in organic synthesis, such as in peptide synthesis and drug synthesis.

Preparation Method:
-Usually, Boc-Asp-OtBu is prepared by reacting the corresponding amino acid (L-glutamic acid) with a tert-butyl protecting group (Boc) and a tert-butoxycarbonyl protecting group (OtBu). The reaction is carried out under suitable conditions, for example by addition of an activator such as 1-(trimethylsilyl)-1H-pyrazol-3-one (TBTU) or N,N'-diisopropylmethylamide (DIPCDI) in an organic solvent.

Safety Information:
- Boc-Asp-OtBu with low toxicity.
-Because it is an organic compound, avoid inhaling dust or contact with skin and eyes.
-When operating, you need to follow appropriate laboratory safety measures, such as wearing protective gloves and eye protection.
-When storing, it should be kept in a cool, dry place, and away from fire and oxidizing agents.

The above content is for reference only, please follow the correct chemical experiment operation specifications when using and handling the Boc-Asp-OtBu.
Last Update:2024-04-09 21:04:16
(S)-4-(叔丁氧基)-3-((叔丁氧基羰基)氨基)-4-氧代丁酸
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