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CAS

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1370641-43-2

(4S)-3-(3-methylbut-1-yn-1-yl)-4-phenyl-1,3-oxazolidin-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1370641-43-2 Structure

  • Basic information

    1. Product Name: (4S)-3-(3-methylbut-1-yn-1-yl)-4-phenyl-1,3-oxazolidin-2-one
    2. Synonyms: (4S)-3-(3-methylbut-1-yn-1-yl)-4-phenyl-1,3-oxazolidin-2-one
    3. CAS NO:1370641-43-2
    4. Molecular Formula:
    5. Molecular Weight: 229.279
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1370641-43-2.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: (4S)-3-(3-methylbut-1-yn-1-yl)-4-phenyl-1,3-oxazolidin-2-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: (4S)-3-(3-methylbut-1-yn-1-yl)-4-phenyl-1,3-oxazolidin-2-one(1370641-43-2)
    11. EPA Substance Registry System: (4S)-3-(3-methylbut-1-yn-1-yl)-4-phenyl-1,3-oxazolidin-2-one(1370641-43-2)

  • 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: 1370641-43-2(Hazardous Substances Data)

1370641-43-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1370641-43-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,0,6,4 and 1 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1370641-43:
(9*1)+(8*3)+(7*7)+(6*0)+(5*6)+(4*4)+(3*1)+(2*4)+(1*3)=142
142 % 10 = 2
So 1370641-43-2 is a valid CAS Registry Number.

1370641-43-2Relevant articles and documents

Preparation method of novel boron-containing adjuvant drug key intermediate chiral alpha-amino borate

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Paragraph 0074-0077, (2020/10/06)

The invention belongs to the technical field of drug synthesis and preparation, and particularly relates to a preparation method of a novel boron-containing adjuvant drug key intermediate chiral alpha-amino borate. The preparation method has the advantages of cheap and easily available raw materials, simple operation, mild reaction, simple post-reaction treatment, high optical purity of the product and the like, the final product does not need to be further purified, the industrialization requirement is met, and the preparation method has very remarkable economic practicability and developmentpotential.

Oxazolidinone-promoted, torquoselective Nazarov cyclizations

Kerr, Daniel J.,Miletic, Michael,Chaplin, Jason H.,White, Jonathan M.,Flynn, Bernard L.

supporting information; experimental part, p. 1732 - 1735 (2012/06/04)

Oxazolidinones are powerful promoters of the Nazarov reaction, enabling the cyclization of conventionally resistant substrates to be achieved under mild conditions. They exert excellent regio-and torquoselective control in both the conventional Nazarov reaction giving cyclopentenones and in the "interrupted" Nazarov reaction, giving more highly substituted multistereocenter containing products.

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