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CAS

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1268165-95-2

(3R)-4-[(4-methylphenyl)sulfonyl]-3-phenylmorpholine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1268165-95-2 Structure

  • Basic information

    1. Product Name: (3R)-4-[(4-methylphenyl)sulfonyl]-3-phenylmorpholine
    2. Synonyms: (3R)-4-[(4-methylphenyl)sulfonyl]-3-phenylmorpholine
    3. CAS NO:1268165-95-2
    4. Molecular Formula:
    5. Molecular Weight: 317.409
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1268165-95-2.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: (3R)-4-[(4-methylphenyl)sulfonyl]-3-phenylmorpholine(CAS DataBase Reference)
    10. NIST Chemistry Reference: (3R)-4-[(4-methylphenyl)sulfonyl]-3-phenylmorpholine(1268165-95-2)
    11. EPA Substance Registry System: (3R)-4-[(4-methylphenyl)sulfonyl]-3-phenylmorpholine(1268165-95-2)

  • 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: 1268165-95-2(Hazardous Substances Data)

1268165-95-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1268165-95-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,8,1,6 and 5 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1268165-95:
(9*1)+(8*2)+(7*6)+(6*8)+(5*1)+(4*6)+(3*5)+(2*9)+(1*5)=182
182 % 10 = 2
So 1268165-95-2 is a valid CAS Registry Number.

1268165-95-2Downstream Products

1268165-95-2Relevant articles and documents

Synthesis of enantiopure 1,4-dioxanes, morpholines, and piperazines from the reaction of chiral 1,2-diols, amino alcohols, and diamines with vinyl selenones

Bagnoli, Luana,Scarponi, Catalina,Rossi, Maria Giovanna,Testaferri, Lorenzo,Tiecco, Marcello

, p. 993 - 999 (2011/03/20)

The reactions of readily available vinyl selenones with enantiopure 1,2-diols, N-protected-1,2-aminoalcohols, and diamines gave substituted enantiopure 1,4-dioxanes, morpholines, and piperazines, respectively, in good to excellent yields. The same procedu

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