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CAS

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1551161-50-2

(S)-N-((1R,2S)-2-hydroxy-1,2-diphenylethyl)azetidine-2-carboxamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1551161-50-2 Structure

  • Basic information

    1. Product Name: (S)-N-((1R,2S)-2-hydroxy-1,2-diphenylethyl)azetidine-2-carboxamide
    2. Synonyms: (S)-N-((1R,2S)-2-hydroxy-1,2-diphenylethyl)azetidine-2-carboxamide
    3. CAS NO:1551161-50-2
    4. Molecular Formula:
    5. Molecular Weight: 296.369
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1551161-50-2.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)-N-((1R,2S)-2-hydroxy-1,2-diphenylethyl)azetidine-2-carboxamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S)-N-((1R,2S)-2-hydroxy-1,2-diphenylethyl)azetidine-2-carboxamide(1551161-50-2)
    11. EPA Substance Registry System: (S)-N-((1R,2S)-2-hydroxy-1,2-diphenylethyl)azetidine-2-carboxamide(1551161-50-2)

  • 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: 1551161-50-2(Hazardous Substances Data)

1551161-50-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1551161-50-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,5,1,1,6 and 1 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1551161-50:
(9*1)+(8*5)+(7*5)+(6*1)+(5*1)+(4*6)+(3*1)+(2*5)+(1*0)=132
132 % 10 = 2
So 1551161-50-2 is a valid CAS Registry Number.

1551161-50-2Downstream Products

1551161-50-2Relevant articles and documents

Enantiopure azetidine-2-carboxamides as organocatalysts for direct asymmetric aldol reactions in aqueous and organic media

Song, Xixi,Liu, Ai-Xiang,Liu, Shan-Shan,Gao, Wen-Chao,Wang, Min-Can,Chang, Junbiao

, p. 1464 - 1470 (2014)

A family of enantiopure azetidine-2-caboxamides was asymmetrically synthesized, and was examined as organocatalyst in direct aldol reactions. A well chosen chiral azetidine-2-caboxamide was found to smoothly catalyze the direct aldol reaction of various benzaldehydes with acetone in brine, and β-hydroxy ketones were produced with enantiomeric excess up to 96%. The reaction of benzaldehydes with cyclic ketones also led to the formation of anti-products in diastereomeric ratio up to 99:1 and enantiomeric excess up to 99%.

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