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Boc-(S)-3-aMino-2-(benzyloxyMethyl)propanoic acid is a chemical compound with the molecular formula C18H23NO5. It is a derivative of the amino acid proline, featuring a Boc (tert-butoxycarbonyl) protecting group on the amino group and a benzyloxymethyl protecting group on the carboxyl group. This unique structure makes it valuable for the preparation of diverse chemical compounds and serves as a chiral intermediate in organic synthesis and pharmaceutical research.

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  • (S)-3-(BENZYLOXY)-2-(((TERT-BUTOXYCARBONYL)AMINO)METHYL)PROPANOIC ACID

    Cas No: 865704-62-7

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  • 865704-62-7 Structure
  • Basic information

    1. Product Name: Boc-(S)-3-aMino-2-(benzyloxyMethyl)propanoic acid
    2. Synonyms: Boc-(S)-3-aMino-2-(benzyloxyMethyl)propanoic acid;(Tert-Butoxy)Carbonyl (S)-3-Amino-2-(benzyloxymethyl)propanoic acid
    3. CAS NO:865704-62-7
    4. Molecular Formula: C16H23NO5
    5. Molecular Weight: 309.35752
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 865704-62-7.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 475.4±45.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.154±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: 2-8°C
    8. Solubility: N/A
    9. PKA: 4.05±0.11(Predicted)
    10. CAS DataBase Reference: Boc-(S)-3-aMino-2-(benzyloxyMethyl)propanoic acid(CAS DataBase Reference)
    11. NIST Chemistry Reference: Boc-(S)-3-aMino-2-(benzyloxyMethyl)propanoic acid(865704-62-7)
    12. EPA Substance Registry System: Boc-(S)-3-aMino-2-(benzyloxyMethyl)propanoic acid(865704-62-7)
  • 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: 865704-62-7(Hazardous Substances Data)

865704-62-7 Usage

Uses

Used in Pharmaceutical Research:
Boc-(S)-3-aMino-2-(benzyloxyMethyl)propanoic acid is used as a chiral intermediate for the development of pharmaceuticals, particularly in the synthesis of biologically active molecules. Its unique structure allows for the creation of various compounds with potential therapeutic applications.
Used in Organic Synthesis:
In the field of organic synthesis, Boc-(S)-3-aMino-2-(benzyloxyMethyl)propanoic acid is utilized as a building block for the synthesis of complex organic molecules. Its versatility and the presence of protecting groups make it an ideal candidate for the preparation of a wide range of chemical compounds.
Used in Peptide Synthesis:
Boc-(S)-3-aMino-2-(benzyloxyMethyl)propanoic acid is employed as a building block in the synthesis of peptides. Its protected structure allows for the stepwise assembly of peptide chains, facilitating the production of peptides with specific sequences and functions.

Check Digit Verification of cas no

The CAS Registry Mumber 865704-62-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,5,7,0 and 4 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 865704-62:
(8*8)+(7*6)+(6*5)+(5*7)+(4*0)+(3*4)+(2*6)+(1*2)=197
197 % 10 = 7
So 865704-62-7 is a valid CAS Registry Number.

865704-62-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name Propanoic acid, 2-[[[(1,1-dimethylethoxy)carbonyl]amino]methyl]-3-(phenylmethoxy)-, (2S)-

1.2 Other means of identification

Product number -
Other names (S)-3-(Benzyloxy)-2-(((tert-butoxycarbonyl)amino)methyl)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:865704-62-7 SDS

865704-62-7Downstream Products

865704-62-7Relevant articles and documents

Chiral succinate: A precursor for enantiomerically pure β2-amino acids

Stoncius, Arvydas,Nahrwold, Markus,Sewald, Norbert

, p. 1829 - 1837 (2007/10/03)

Five suitably protected enantiomerically pure β2-amino acids, homologues of proteinogenic α-amino acids, were synthesized from the common chiral precursor, tert-butyl succinyloxazolidinone. Georg Thieme Verlag Stuttgart.

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