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CAS

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91467-14-0

2,4-Oxazolidinedione, 5,5-dichloro-3-[(2-chlorophenyl)methyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 91467-14-0 Structure

  • Basic information

    1. Product Name: 2,4-Oxazolidinedione, 5,5-dichloro-3-[(2-chlorophenyl)methyl]-
    2. Synonyms:
    3. CAS NO:91467-14-0
    4. Molecular Formula: C10H6Cl3NO3
    5. Molecular Weight: 294.522
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 91467-14-0.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: 2,4-Oxazolidinedione, 5,5-dichloro-3-[(2-chlorophenyl)methyl]-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,4-Oxazolidinedione, 5,5-dichloro-3-[(2-chlorophenyl)methyl]-(91467-14-0)
    11. EPA Substance Registry System: 2,4-Oxazolidinedione, 5,5-dichloro-3-[(2-chlorophenyl)methyl]-(91467-14-0)

  • 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: 91467-14-0(Hazardous Substances Data)

91467-14-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 91467-14-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,4,6 and 7 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 91467-14:
(7*9)+(6*1)+(5*4)+(4*6)+(3*7)+(2*1)+(1*4)=140
140 % 10 = 0
So 91467-14-0 is a valid CAS Registry Number.

91467-14-0Downstream Products

91467-14-0Relevant articles and documents

Reaction of Oxalyl Chloride and Alkyloxalyl Chlorides with Isocyanates and Isothiocyanates

Richter, R.,Stuber, F. A.,Tucker, B.

, p. 3675 - 3681 (2007/10/02)

Alkyl and aryl isothiocyanates react with oxalyl chloride (1) on both double bonds of the heterocumulene to yield 3-alkyl- or 3-aryl-2,2-dichlorothiazolidine-4,5-diones 2.The two chlorines in these novel orthocarbonic acid derivatives are readily exchanged by alkoxy groups to yield 2,2-dialkoxythiazolidine-4,5-diones 3; hydrolysis of 2a (R=CH3) gave 3-methylthiazolidine-2,4,5-trione. 3-Substituted 5,5-dichlorooxazolidine-2,4-diones 8 and 5-chloro-5-alkoxyoxazolidine-2,4-diones 13 are obtained on reacting alkyl, aryl, and benzyl isocyanates with 1 and alkyloxalyl chloride, respectively.Structure assignment to these novel cycloadducts is based on IR, 1H NMR, and 13C NMR spectroscopic as well as X-ray crystallographic analysis.Formation of 8 and 13 is a stepwise process involving labile acyclic intermediates 7 and 12.The cyclizations to 8 and 13 take place only on the C=N bond of the isocyanate group.

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