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365552-27-8

2-Pyrrolidinecarboxamide,N-(2-hydroxyethyl)-5-oxo-,(2S)-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 365552-27-8 Structure

  • Basic information

    1. Product Name: 2-Pyrrolidinecarboxamide,N-(2-hydroxyethyl)-5-oxo-,(2S)-(9CI)
    2. Synonyms: 2-Pyrrolidinecarboxamide,N-(2-hydroxyethyl)-5-oxo-,(2S)-(9CI)
    3. CAS NO:365552-27-8
    4. Molecular Formula: C7H12N2O3
    5. Molecular Weight: 0
    6. EINECS: N/A
    7. Product Categories: PYRROLE
    8. Mol File: 365552-27-8.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-Pyrrolidinecarboxamide,N-(2-hydroxyethyl)-5-oxo-,(2S)-(9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Pyrrolidinecarboxamide,N-(2-hydroxyethyl)-5-oxo-,(2S)-(9CI)(365552-27-8)
    11. EPA Substance Registry System: 2-Pyrrolidinecarboxamide,N-(2-hydroxyethyl)-5-oxo-,(2S)-(9CI)(365552-27-8)

  • 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: 365552-27-8(Hazardous Substances Data)

365552-27-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 365552-27-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,6,5,5,5 and 2 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 365552-27:
(8*3)+(7*6)+(6*5)+(5*5)+(4*5)+(3*2)+(2*2)+(1*7)=158
158 % 10 = 8
So 365552-27-8 is a valid CAS Registry Number.

365552-27-8Downstream Products

365552-27-8Relevant articles and documents

Five- and six-membered ring opening of pyroglutamic diketopiperazine

Parrish, Dennis A.,Mathias, Lon J.

, p. 1820 - 1826 (2007/10/03)

A variety of ring-opening reactions of pyroglutamic diketopiperazine at both the five-membered and six-membered rings is described. Mild, basic conditions facilitate nucleophilic attack by amines at the diketopiperazine carbonyls giving pyroglutamides in excellent yield. Reaction with nucleophiles under acidic conditions give bis-glutamate derivatives of 2,5-diketopiperazine (DKP). These reactions provide simple, two-step sequences to pyroglutamides and symmetrical diketopiperazines from commercial pyroglutamic acid with control of product dictated by reaction conditions, catalyst, and nucleophile.

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