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1422064-40-1

1-[4-(4-methoxybutoxy)benzyl]-5-oxo-L-prolyl-L-histidine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1422064-40-1 Structure

  • Basic information

    1. Product Name: 1-[4-(4-methoxybutoxy)benzyl]-5-oxo-L-prolyl-L-histidine
    2. Synonyms: 1-[4-(4-methoxybutoxy)benzyl]-5-oxo-L-prolyl-L-histidine
    3. CAS NO:1422064-40-1
    4. Molecular Formula:
    5. Molecular Weight: 458.514
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1422064-40-1.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: 1-[4-(4-methoxybutoxy)benzyl]-5-oxo-L-prolyl-L-histidine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-[4-(4-methoxybutoxy)benzyl]-5-oxo-L-prolyl-L-histidine(1422064-40-1)
    11. EPA Substance Registry System: 1-[4-(4-methoxybutoxy)benzyl]-5-oxo-L-prolyl-L-histidine(1422064-40-1)

  • 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: 1422064-40-1(Hazardous Substances Data)

1422064-40-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1422064-40-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,2,0,6 and 4 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1422064-40:
(9*1)+(8*4)+(7*2)+(6*2)+(5*0)+(4*6)+(3*4)+(2*4)+(1*0)=111
111 % 10 = 1
So 1422064-40-1 is a valid CAS Registry Number.

1422064-40-1Downstream Products

1422064-40-1Relevant articles and documents

Synthesis of new optically active 2-pyrrolidinones

Moutevelis-Minakakis, Panagiota,Papavassilopoulou, Eleni,Mavromoustakos, Thomas

, p. 50 - 73 (2013/03/14)

A new class of optically active 2-pyrrolidinones was synthesized, starting from S-pyroglutamic acid, a well known natural chiral synthon. The synthetic design followed led to the insertion of various substituents at positions 1 and 5 of the 2-pyrrolidinone ring, including the imidazole moiety. Some of them possess two or three stereogenic centers, the configuration of which was retained under the mild conditions used. The new compounds also carry an imidazole moiety, which, along with the 2-pyrrolidinone template, may prove pivotal to several biological processes.

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