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1430204-29-7

Fmoc-Aib-Gly-Pro is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1430204-29-7 Structure

  • Basic information

    1. Product Name: Fmoc-Aib-Gly-Pro
    2. Synonyms: Fmoc-Aib-Gly-Pro
    3. CAS NO:1430204-29-7
    4. Molecular Formula:
    5. Molecular Weight: 479.533
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1430204-29-7.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Fmoc-Aib-Gly-Pro(CAS DataBase Reference)
    10. NIST Chemistry Reference: Fmoc-Aib-Gly-Pro(1430204-29-7)
    11. EPA Substance Registry System: Fmoc-Aib-Gly-Pro(1430204-29-7)

  • 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: 1430204-29-7(Hazardous Substances Data)

1430204-29-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1430204-29-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,3,0,2,0 and 4 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1430204-29:
(9*1)+(8*4)+(7*3)+(6*0)+(5*2)+(4*0)+(3*4)+(2*2)+(1*9)=97
97 % 10 = 7
So 1430204-29-7 is a valid CAS Registry Number.

1430204-29-7Downstream Products

1430204-29-7Relevant articles and documents

Use of an internal reference for the quantitative HPLC-UV analysis of solid-phase reactions: A case study of 2-chlorotrityl chloride resin

Spengler, Jan,Fernandez-Llamazares, Anna-Iris,Albericio, Fernando

, p. 229 - 234 (2013)

Here we evaluated the use of internal reference compounds for the rapid assessment of reactions performed in solid-phase. An internal reference compound (commercially available) was bound to the resin, together with the substrate, and cleaved with the products after completion of the reaction. The peak area of the reference compound in the HPLC-UV chromatograms can be correlated directly with those of other compounds present in the reaction mixture, thereby allowing a quantitative interpretation of the chromatograms with respect to conversion and yield. The usefulness of this method was demonstrated by optimization of a protocol for the synthesis of proline-based tripeptides.

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