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CAS

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1522125-09-2

(S)-2-benzamido-3-((4-methoxyphenethyl)amino)-3-oxopropyl monobenzyl dihydrogen diphosphate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1522125-09-2 Structure

  • Basic information

    1. Product Name: (S)-2-benzamido-3-((4-methoxyphenethyl)amino)-3-oxopropyl monobenzyl dihydrogen diphosphate
    2. Synonyms:
    3. CAS NO:1522125-09-2
    4. Molecular Formula:
    5. Molecular Weight: 598.412
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1522125-09-2.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-benzamido-3-((4-methoxyphenethyl)amino)-3-oxopropyl monobenzyl dihydrogen diphosphate(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S)-2-benzamido-3-((4-methoxyphenethyl)amino)-3-oxopropyl monobenzyl dihydrogen diphosphate(1522125-09-2)
    11. EPA Substance Registry System: (S)-2-benzamido-3-((4-methoxyphenethyl)amino)-3-oxopropyl monobenzyl dihydrogen diphosphate(1522125-09-2)

  • 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: 1522125-09-2(Hazardous Substances Data)

1522125-09-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1522125-09-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,2,2,1,2 and 5 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1522125-09:
(9*1)+(8*5)+(7*2)+(6*2)+(5*1)+(4*2)+(3*5)+(2*0)+(1*9)=112
112 % 10 = 2
So 1522125-09-2 is a valid CAS Registry Number.

1522125-09-2Downstream Products

1522125-09-2Relevant articles and documents

Chemical pyrophosphorylation of functionally diverse peptides

Marmelstein, Alan M.,Yates, Lisa M.,Conway, John H.,Fiedler, Dorothea

, p. 108 - 111 (2014/01/23)

A highly selective and convenient method for the synthesis of pyrophosphopeptides in solution is reported. The remarkable compatibility with functional groups (alcohol, thiol, amine, carboxylic acid) in the peptide substrates suggests that the intrinsic nucleophilicity of the phosphoserine residue is much higher than previously appreciated. Because the methodology operates in polar solvents, including water, a broad range of pyrophosphopeptides can be accessed. We envision these peptides will find widespread applications in the development of mass spectrometry and antibody-based detection methods for pyrophosphoproteins.

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