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(S)-2-(9H-Fluoren-9-ylmethoxycarbonylamino)-3-(5-hydroxy-pyridin-2-yl)-propionic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 206446-52-8 Structure
  • Basic information

    1. Product Name: (S)-2-(9H-Fluoren-9-ylmethoxycarbonylamino)-3-(5-hydroxy-pyridin-2-yl)-propionic acid
    2. Synonyms:
    3. CAS NO:206446-52-8
    4. Molecular Formula:
    5. Molecular Weight: 404.422
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 206446-52-8.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: (S)-2-(9H-Fluoren-9-ylmethoxycarbonylamino)-3-(5-hydroxy-pyridin-2-yl)-propionic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S)-2-(9H-Fluoren-9-ylmethoxycarbonylamino)-3-(5-hydroxy-pyridin-2-yl)-propionic acid(206446-52-8)
    11. EPA Substance Registry System: (S)-2-(9H-Fluoren-9-ylmethoxycarbonylamino)-3-(5-hydroxy-pyridin-2-yl)-propionic acid(206446-52-8)
  • 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: 206446-52-8(Hazardous Substances Data)

206446-52-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 206446-52-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,6,4,4 and 6 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 206446-52:
(8*2)+(7*0)+(6*6)+(5*4)+(4*4)+(3*6)+(2*5)+(1*2)=118
118 % 10 = 8
So 206446-52-8 is a valid CAS Registry Number.

206446-52-8Downstream Products

206446-52-8Relevant articles and documents

Preparation of phospho-L-azatyrosine suitably protected for the synthesis of signal transduction related peptides. A correction

Yao, Zhu-Jun,Ye, Bin,Miyoshi, Kengo,Otaka, Akira,Burke Jr., Terrence R.

, p. 428 - 430 (1998)

Synthesis of Nα-Fmoc 4-O,O-(di-tert-butyl)phospho-L-azatyrosine (6) and its use in Fmoc-based solid-phase peptide synthesis are reported. The di-tert-butyl phospho protecting groups were removed during TFA-mediated cleavage of the finished peptide (10) from the resin, providing the free phosphoazatyrosine-containing peptide directly. This is in contrast to diethyl phospho protection we previously reported [Ye, B.; Otaka, A.; Burke, T. R., Jr. Synlett. 1996, 459-460] in which the diethyl protection has proven impractical to remove. Due to incorrect assignment of starting material, the title compound of this latter report should be corrected to the isomeric L-β-(3-hydroxy-2-pyridyl)-alanine compound (5).

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