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406220-07-3

(1R,4'S,5'S/1S,4'S,5'S)-2-(1-chloroethyl)-4-methoxymethyl-5-phenyl-2-oxazoline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 406220-07-3 Structure

  • Basic information

    1. Product Name: (1R,4'S,5'S/1S,4'S,5'S)-2-(1-chloroethyl)-4-methoxymethyl-5-phenyl-2-oxazoline
    2. Synonyms: (1R,4'S,5'S/1S,4'S,5'S)-2-(1-chloroethyl)-4-methoxymethyl-5-phenyl-2-oxazoline
    3. CAS NO:406220-07-3
    4. Molecular Formula:
    5. Molecular Weight: 253.729
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 406220-07-3.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: (1R,4'S,5'S/1S,4'S,5'S)-2-(1-chloroethyl)-4-methoxymethyl-5-phenyl-2-oxazoline(CAS DataBase Reference)
    10. NIST Chemistry Reference: (1R,4'S,5'S/1S,4'S,5'S)-2-(1-chloroethyl)-4-methoxymethyl-5-phenyl-2-oxazoline(406220-07-3)
    11. EPA Substance Registry System: (1R,4'S,5'S/1S,4'S,5'S)-2-(1-chloroethyl)-4-methoxymethyl-5-phenyl-2-oxazoline(406220-07-3)

  • 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: 406220-07-3(Hazardous Substances Data)

406220-07-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 406220-07-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,6,2,2 and 0 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 406220-07:
(8*4)+(7*0)+(6*6)+(5*2)+(4*2)+(3*0)+(2*0)+(1*7)=93
93 % 10 = 3
So 406220-07-3 is a valid CAS Registry Number.

406220-07-3Downstream Products

406220-07-3Relevant articles and documents

Lithiation of 2-(1-chloroethyl)-2-oxazolines: Synthesis of substituted oxazolinyloxiranes and oxazolinylaziridines

Capriati,Degennaro,Florio,Luisi,Tralli,Troisi

, p. 2299 - 2306 (2001)

Lithiation of 2-(1-chloroethyl)-4,4-dimethyl-2-oxazoline 2 leads to lithiated derivative 3, which is quite stable and can be deuterated, methylated and silylated to give oxazolines 4a-c. The reaction of 3 with carbonyl compounds and imines furnishes good to excellent yields of oxazolinylepoxides 6a-m and aziridines 17a-f, respectively. Methylation and NaBH4 reduction of epoxides 6 afford oxazolidines 7 highly stereoselectively. Acylepoxides can be obtained by hydrolysis of the oxazolidine moiety.

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