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127902-98-1

Staphyloferrin A is a D-ornithine derivative that is formed by the formal condensation of the terminal carboxy groups of two citric acid units with the two amino groups of D-ornithine. It is a unique compound with potential applications in various fields due to its distinct chemical properties.

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  • Butanedioic acid,2-[2-[[(1R)-1-carboxy-4-[[(3S)-3,4-dicarboxy-3-hydroxy-1-oxobutyl]amino]butyl]amino]-2-oxoethyl]-2-hydroxy-,(2S)-

    Cas No: 127902-98-1

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  • Butanedioic acid,2-[2-[[(1R)-1-carboxy-4-[[(3S)-3,4-dicarboxy-3-hydroxy-1-oxobutyl]amino]butyl]amino]-2-oxoethyl]-2-hydroxy-,(2S)-

    Cas No: 127902-98-1

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  • 2-[2-[[4-carboxy-4-[(3,4-dicarboxy-3-hydroxybutanoyl)amino]butyl]amino]-2-oxoethyl]-2-hydroxybutanedioic acid

    Cas No: 127902-98-1

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  • 127902-98-1 Structure

  • Basic information

    1. Product Name: staphyloferrin A
    2. Synonyms: staphyloferrin A
    3. CAS NO:127902-98-1
    4. Molecular Formula: C17H24N2O14
    5. Molecular Weight: 480.38
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 127902-98-1.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 949.4°Cat760mmHg
    3. Flash Point: 528°C
    4. Appearance: /
    5. Density: 1.658g/cm3
    6. Vapor Pressure: 0mmHg at 25°C
    7. Refractive Index: 1.598
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: staphyloferrin A(CAS DataBase Reference)
    11. NIST Chemistry Reference: staphyloferrin A(127902-98-1)
    12. EPA Substance Registry System: staphyloferrin A(127902-98-1)

  • 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: 127902-98-1(Hazardous Substances Data)

127902-98-1 Usage

Uses

Used in Pharmaceutical Industry:
Staphyloferrin A is used as a pharmaceutical compound for its potential therapeutic applications. The expression is: staphyloferrin A is used as a therapeutic agent for its unique chemical properties and potential to target specific biological processes.
Used in Research and Development:
In the field of research and development, staphyloferrin A is used as a chemical compound for studying its interactions with other molecules and understanding its potential applications in drug discovery and development. The expression is: staphyloferrin A is used as a research compound for exploring its interactions and potential applications in drug discovery.
Used in Diagnostic Applications:
Staphyloferrin A may also find use in diagnostic applications, where its unique properties can be utilized to develop new diagnostic tools or enhance existing ones. The expression is: staphyloferrin A is used as a diagnostic agent for its potential to improve diagnostic tools and techniques.

Check Digit Verification of cas no

The CAS Registry Mumber 127902-98-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,9,0 and 2 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 127902-98:
(8*1)+(7*2)+(6*7)+(5*9)+(4*0)+(3*2)+(2*9)+(1*8)=141
141 % 10 = 1
So 127902-98-1 is a valid CAS Registry Number.
InChI:InChI=1/C17H24N2O14/c20-9(4-16(32,14(28)29)6-11(22)23)18-3-1-2-8(13(26)27)19-10(21)5-17(33,15(30)31)7-12(24)25/h8,32-33H,1-7H2,(H,18,20)(H,19,21)(H,22,23)(H,24,25)(H,26,27)(H,28,29)(H,30,31)

127902-98-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name staphyloferrin A

1.2 Other means of identification

Product number -
Other names 2-[2-[[4-carboxy-4-[(3,4-dicarboxy-3-hydroxybutanoyl)amino]butyl]amino]-2-oxoethyl]-2-hydroxybutanedioic 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:127902-98-1 SDS

127902-98-1Downstream Products

127902-98-1Relevant articles and documents

Streamlined synthesis of (R, R)-rhizoferrin, (S, S)-rhizoferrin and (R, S, R)-staphyloferrin A

Csuk, René,Deising, Holger B.,Raschke, Anja,Serbian, Immo,Wiese, Jana

, p. 64 - 69 (2019)

(R, R)-Rhizoferrin and (R, S, R)-staphyloferrin A are carboxylate-type siderophores. Their streamlined synthesis has been accomplished starting from (R)-citric acid. Key-step of these syntheses is a chemo-enzymatic ester hydrolysis. (S, S)-rhizoferrin was accessible by a multistep synthesis starting from an (S)-citrate derived synthon.

Chemical synthesis of staphyloferrin A and its application for Staphylococcus aureus detection

Pandey, Rajesh K.,Jarvis, Gregory G.,Low, Philip S.

, p. 1707 - 1710 (2014/03/21)

The chemical synthesis of staphyloferrin A, a siderophore used by Staphylococcus bacteria for ferric iron retrieval, has been achieved with 79% yield via solid phase peptide synthesis (SPPS). Biological activity of synthetic staphyloferrin A has been confirmed by demonstrating its capture and uptake by live S. aureus.

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