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CAS

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249610-99-9

(2S,4S,5R)-(-)-Methyl 3-(2-chloroacetyl)-5-methyl-2-phenyl-1,3-oxazolidine-4-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 249610-99-9 Structure

  • Basic information

    1. Product Name: (2S,4S,5R)-(-)-Methyl 3-(2-chloroacetyl)-5-methyl-2-phenyl-1,3-oxazolidine-4-carboxylate
    2. Synonyms: (2S,4S,5R)-(-)-Methyl 3-(2-chloroacetyl)-5-methyl-2-phenyl-1,3-oxazolidine-4-carboxylate
    3. CAS NO:249610-99-9
    4. Molecular Formula:
    5. Molecular Weight: 297.738
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 249610-99-9.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: (2S,4S,5R)-(-)-Methyl 3-(2-chloroacetyl)-5-methyl-2-phenyl-1,3-oxazolidine-4-carboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2S,4S,5R)-(-)-Methyl 3-(2-chloroacetyl)-5-methyl-2-phenyl-1,3-oxazolidine-4-carboxylate(249610-99-9)
    11. EPA Substance Registry System: (2S,4S,5R)-(-)-Methyl 3-(2-chloroacetyl)-5-methyl-2-phenyl-1,3-oxazolidine-4-carboxylate(249610-99-9)

  • 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: 249610-99-9(Hazardous Substances Data)

249610-99-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 249610-99-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,9,6,1 and 0 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 249610-99:
(8*2)+(7*4)+(6*9)+(5*6)+(4*1)+(3*0)+(2*9)+(1*9)=159
159 % 10 = 9
So 249610-99-9 is a valid CAS Registry Number.

249610-99-9Relevant articles and documents

A facile synthesis of enantiomerically pure 1-(piperazin-2-yl)ethan-1-ol derivatives from (2s,3r)-threonine

Soukara, Stella,Wuensch, Bernhard

, p. 1739 - 1746 (1999)

Starting from the proteinogenic amino acid (2S,3R)-threonine (4) a novel method for the preparation of enantiomerically pure 1-(1-benzylpiperazin-2- yl)ethan-1-ols with various substituents in position 4 (15 - 20) is described. The sequence involves as key step the LiAlH4 reduction of the bicyclic piperazinediones 11a,b-14a,b which establishes the 1-benzyl protective group and simultaneously liberates the 1-hydroxyethyl side chain for further transformations.

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