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1262957-05-0

(S)-N-(1-hydroxy-3-phenylpropan-2-yl)-2-(1H-benzo[d]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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  • 1262957-05-0 Structure

  • Basic information

    1. Product Name: (S)-N-(1-hydroxy-3-phenylpropan-2-yl)-2-(1H-benzo[d]imidazol-1-yl)acetamide
    2. Synonyms: (S)-N-(1-hydroxy-3-phenylpropan-2-yl)-2-(1H-benzo[d]imidazol-1-yl)acetamide
    3. CAS NO:1262957-05-0
    4. Molecular Formula:
    5. Molecular Weight: 309.368
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1262957-05-0.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)-N-(1-hydroxy-3-phenylpropan-2-yl)-2-(1H-benzo[d]imidazol-1-yl)acetamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S)-N-(1-hydroxy-3-phenylpropan-2-yl)-2-(1H-benzo[d]imidazol-1-yl)acetamide(1262957-05-0)
    11. EPA Substance Registry System: (S)-N-(1-hydroxy-3-phenylpropan-2-yl)-2-(1H-benzo[d]imidazol-1-yl)acetamide(1262957-05-0)

  • 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: 1262957-05-0(Hazardous Substances Data)

1262957-05-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1262957-05-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,2,9,5 and 7 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1262957-05:
(9*1)+(8*2)+(7*6)+(6*2)+(5*9)+(4*5)+(3*7)+(2*0)+(1*5)=170
170 % 10 = 0
So 1262957-05-0 is a valid CAS Registry Number.

1262957-05-0Downstream Products

1262957-05-0Relevant articles and documents

A new C2-symmetric azolium compound for Cu-catalyzed asymmetric conjugate addition of R2Zn to cyclic enone

Harano, Ayako,Sakaguchi, Satoshi

, p. 61 - 67 (2011)

A new chiral N-heterocyclic carbene (NHC) ligand was designed. Thus, an efficient synthetic route to C2-symmetric bis(hydroxyamide)- functionalized benzimidazolium salts from chiral β-amino alcohols was developed. The combination of Cu(OTf)sub

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 (2015/02/02)

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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