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1153125-92-8

N-(2-hydroxyethyl)-2-(1H-imidazol-1-yl)acetamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1153125-92-8 Structure

  • Basic information

    1. Product Name: N-(2-hydroxyethyl)-2-(1H-imidazol-1-yl)acetamide
    2. Synonyms: N-(2-hydroxyethyl)-2-(1H-imidazol-1-yl)acetamide
    3. CAS NO:1153125-92-8
    4. Molecular Formula:
    5. Molecular Weight: 169.183
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1153125-92-8.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: N-(2-hydroxyethyl)-2-(1H-imidazol-1-yl)acetamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(2-hydroxyethyl)-2-(1H-imidazol-1-yl)acetamide(1153125-92-8)
    11. EPA Substance Registry System: N-(2-hydroxyethyl)-2-(1H-imidazol-1-yl)acetamide(1153125-92-8)

  • 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: 1153125-92-8(Hazardous Substances Data)

1153125-92-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1153125-92-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,5,3,1,2 and 5 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1153125-92:
(9*1)+(8*1)+(7*5)+(6*3)+(5*1)+(4*2)+(3*5)+(2*9)+(1*2)=118
118 % 10 = 8
So 1153125-92-8 is a valid CAS Registry Number.

1153125-92-8Downstream Products

1153125-92-8Relevant articles and documents

Synthesis of β-hydroxyacetamides from unactivated ethyl acetates under base-free conditions and microwave irradiation

Hernández-Fernández, Eugenio,Sánchez-Lara, Pedro Pablo,Ordó?ez, Mario,Ramírez-Marroquín, Oscar Abelardo,Avalos-Alanís, Francisco G.,López-Cortina, Susana,Jiménez-Pérez, Víctor M.,Ibarra-Rivera, Tannya Rocio

, p. 73 - 78 (2015)

The amidation of unactivated ethyl esters with achiral and chiral 1,2-amino alcohols under microwave irradiation and base-free conditions is described. This procedure provides a convenient method for the synthesis of β-hydroxyacetamides bearing pyrazole, imidazole, and benzimidazole groups in high yields and without racemization. The protocol described herein is environmentally friendly and allows for the preparation of a wide variety of β-hydroxyacetamides, which are key intermediates in the synthesis of oxazolines and other derivatives of biological interest.

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