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172299-81-9

N-Boc-N-methoxy-3-aminopropionic acid is a complex organic chemical compound that features an amine, carboxylic acid, and an ester functional groups. It is a derivative of aminopropionic acid, distinguished by the presence of an N-Boc (tert-butoxycarbonyl) protecting group, which shields the amino group during chemical reactions. This feature renders it a valuable asset in organic synthesis. Additionally, the methoxy group in the compound contributes to its stability.

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  • SAGECHEM/3-((tert-Butoxycarbonyl)(methoxy)amino)propanoic acid/SAGECHEM/Manufacturer in China

    Cas No: 172299-81-9

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  • 172299-81-9 Structure

  • Basic information

    1. Product Name: N-Boc-N-methoxy-3-aminopropionic acid
    2. Synonyms: N-Boc-N-methoxy-3-aminopropionic acid;3-(Tert-butoxycarbonyl(methoxy)amino)propanoic acid;b-Alanine,N-[(1,1-diMethylethoxy)carbonyl]-N-Methoxy-;N-[(1,1-Dimethylethoxy)carbonyl]-N-methoxy-beta-alanine
    3. CAS NO:172299-81-9
    4. Molecular Formula: C9H17NO5
    5. Molecular Weight: 219.24
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 172299-81-9.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 327.789 °C at 760 mmHg
    3. Flash Point: 152.042 °C
    4. Appearance: /
    5. Density: 1.161g/cm3
    6. Refractive Index: N/A
    7. Storage Temp.: 2-8°C
    8. Solubility: N/A
    9. PKA: 4.46±0.10(Predicted)
    10. CAS DataBase Reference: N-Boc-N-methoxy-3-aminopropionic acid(CAS DataBase Reference)
    11. NIST Chemistry Reference: N-Boc-N-methoxy-3-aminopropionic acid(172299-81-9)
    12. EPA Substance Registry System: N-Boc-N-methoxy-3-aminopropionic acid(172299-81-9)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 172299-81-9(Hazardous Substances Data)

172299-81-9 Usage

Uses

Used in Medicinal Chemistry:
N-Boc-N-methoxy-3-aminopropionic acid is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its protective N-Boc group and the stability provided by the methoxy group make it a preferred choice for the development of drugs and pharmaceuticals.
Used in Organic Synthesis:
In the field of organic synthesis, N-Boc-N-methoxy-3-aminopropionic acid is used as a building block for the creation of more complex molecules. The N-Boc protecting group allows for selective reactions, facilitating the synthesis of target compounds with greater precision and control.
Storage:
N-Boc-N-methoxy-3-aminopropionic acid should be stored under standard laboratory conditions, such as at room temperature and atmospheric pressure, to maintain its stability and ensure its reactivity in subsequent chemical reactions.

Check Digit Verification of cas no

The CAS Registry Mumber 172299-81-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,2,2,9 and 9 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 172299-81:
(8*1)+(7*7)+(6*2)+(5*2)+(4*9)+(3*9)+(2*8)+(1*1)=159
159 % 10 = 9
So 172299-81-9 is a valid CAS Registry Number.

172299-81-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-((tert-Butoxycarbonyl)(methoxy)amino)propanoic acid

1.2 Other means of identification

Product number -
Other names 3-[methoxy-[(2-methylpropan-2-yl)oxycarbonyl]amino]propanoic acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:172299-81-9 SDS

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172299-81-9Relevant articles and documents

Solid Phase Synthesis of C-Terminal Peptide Aldehydes

Fehrentz,Paris,Heitz,Velek,Winternitz,Martinez

, p. 6792 - 6796 (1997)

Peptides with C-terminal aldehydes (PAs) are of interest due to their inhibitory properties toward numerous classes of proteolytic enzymes. In this paper, we describe and compare two novel approaches for the preparation of PAs by solid phase synthesis, on

Improved solid phase synthesis of C-terminal peptide aldehydes

Fehrentz, Jean-Alain,Paris, Marielle,Heitz, Annie,Velek, Jiri,Liu, Chuan-Fa,et al.

, p. 7871 - 7874 (1995)

A new linker based on the Weinreb amide was developed in order to synthesize from peptidyl-resin the corresponding aldehydic peptides by reduction with LiAlH4.This new reaction was tested with N-protected amino-residues and with tripeptides to obtain the

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