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84967-68-0

3-benzoyl-5,5-dimethyl-2-oxazolidinone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 84967-68-0 Structure

  • Basic information

    1. Product Name: 3-benzoyl-5,5-dimethyl-2-oxazolidinone
    2. Synonyms: 3-benzoyl-5,5-dimethyl-2-oxazolidinone
    3. CAS NO:84967-68-0
    4. Molecular Formula:
    5. Molecular Weight: 219.24
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 84967-68-0.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: 3-benzoyl-5,5-dimethyl-2-oxazolidinone(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-benzoyl-5,5-dimethyl-2-oxazolidinone(84967-68-0)
    11. EPA Substance Registry System: 3-benzoyl-5,5-dimethyl-2-oxazolidinone(84967-68-0)

  • 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: 84967-68-0(Hazardous Substances Data)

84967-68-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84967-68-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,9,6 and 7 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 84967-68:
(7*8)+(6*4)+(5*9)+(4*6)+(3*7)+(2*6)+(1*8)=190
190 % 10 = 0
So 84967-68-0 is a valid CAS Registry Number.

84967-68-0Downstream Products

84967-68-0Relevant articles and documents

Synthesis of Chiral Selenazolines from N-Acyloxazolidinones via a Selenative Rearrangement of Chiral Cyclic Skeletons

Shibahara, Fumitoshi,Fukunaga, Tomoki,Kubota, Saki,Yoshida, Akihito,Murai, Toshiaki

, p. 5826 - 5830 (2018)

A synthetic route to chiral selenazolines from readily available N-acyloxazolidinones via a selenative rearrangement of a chiral cyclic skeleton is reported. The reaction proceeds in the presence of elemental selenium, a hydrochlorosilane, and an amine. A

Cyclization Reactions of β,γ-Unsaturated Derivatives of Carbonic Acid. VII. Synthesis of Unequivocal N-Acylated Thiazolidine-2-ones and Oxazolidine-2-ones

Widera, R.,Muehlstaedt, M.

, p. 1005 - 1010 (2007/10/02)

A new synthetic route to N-acylated thiazolidine-2-ones and oxazolidine-2-ones is reported: The reaction of carboxylic acid chlorides with 2-alkoxy-2-thiazolines (1,2) or -2-oxazolines (3) yields unequivocal N-acylated thiazolidine-2-ones (4-6) or oxazolidine-2-ones (7).Bifunctional acid chlorides, e.g. oxalyl chloride or thiophosgene yield compounds 11 and 12.

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