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CAS

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1374255-89-6

(S)-N-[3-(benzyloxy)-4-hydroxybutyl]-2,2,2-trifluoroacetamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1374255-89-6 Structure

  • Basic information

    1. Product Name: (S)-N-[3-(benzyloxy)-4-hydroxybutyl]-2,2,2-trifluoroacetamide
    2. Synonyms: (S)-N-[3-(benzyloxy)-4-hydroxybutyl]-2,2,2-trifluoroacetamide
    3. CAS NO:1374255-89-6
    4. Molecular Formula:
    5. Molecular Weight: 291.27
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1374255-89-6.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-[3-(benzyloxy)-4-hydroxybutyl]-2,2,2-trifluoroacetamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S)-N-[3-(benzyloxy)-4-hydroxybutyl]-2,2,2-trifluoroacetamide(1374255-89-6)
    11. EPA Substance Registry System: (S)-N-[3-(benzyloxy)-4-hydroxybutyl]-2,2,2-trifluoroacetamide(1374255-89-6)

  • 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: 1374255-89-6(Hazardous Substances Data)

1374255-89-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1374255-89-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,4,2,5 and 5 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1374255-89:
(9*1)+(8*3)+(7*7)+(6*4)+(5*2)+(4*5)+(3*5)+(2*8)+(1*9)=176
176 % 10 = 6
So 1374255-89-6 is a valid CAS Registry Number.

1374255-89-6Relevant articles and documents

Synthesis of chiral five-, six-, and seven-membered heterocycles from (S)-3-hydroxy-γ-butyrolactone

Yang, Hao,Goyal, Navneet,Ella-Menye, Jean Rene,Williams, Kristopher,Wang, Guijun

, p. 561 - 568 (2012/05/05)

Chiral small molecules such as amino alcohols and their heterocyclic derivatives are useful building blocks for asymmetric synthesis and the preparation of biologically active compounds. Using a common starting material derived from carbohydrate, the (S)-3-hydroxy - butyrolactone, we have synthesized several five-, six-, and seven-membered nitrogen-containing chiral heterocycles. These include (S)-3-benzyloxypyrrolidine, a protected 6-substituted morpholin-3-one and its homologous 1,4-oxazepan-3-one, and 6-trityloxymethyl tetrahydro-1,3-oxazine-2-thiones. These chiral small heterocycles were synthesized from the lactone via efficient cyclization reactions. Their syntheses and characterization are reported here. Georg Thieme Verlag Stuttgart - New York.

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