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CAS

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211096-32-1

Isoxazole, 4-(2-furanyl)-3,5-dimethyl- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 211096-32-1 Structure

  • Basic information

    1. Product Name: Isoxazole, 4-(2-furanyl)-3,5-dimethyl- (9CI)
    2. Synonyms: Isoxazole, 4-(2-furanyl)-3,5-dimethyl- (9CI)
    3. CAS NO:211096-32-1
    4. Molecular Formula: C9H9NO2
    5. Molecular Weight: 163.17326
    6. EINECS: N/A
    7. Product Categories: OXAZOLE
    8. Mol File: 211096-32-1.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Isoxazole, 4-(2-furanyl)-3,5-dimethyl- (9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: Isoxazole, 4-(2-furanyl)-3,5-dimethyl- (9CI)(211096-32-1)
    11. EPA Substance Registry System: Isoxazole, 4-(2-furanyl)-3,5-dimethyl- (9CI)(211096-32-1)

  • 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: 211096-32-1(Hazardous Substances Data)

211096-32-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 211096-32-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,1,0,9 and 6 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 211096-32:
(8*2)+(7*1)+(6*1)+(5*0)+(4*9)+(3*6)+(2*3)+(1*2)=91
91 % 10 = 1
So 211096-32-1 is a valid CAS Registry Number.

211096-32-1Downstream Products

211096-32-1Relevant articles and documents

Synthesis of sulfonate derivatives of 4-heteryl-isoxazoles

Shumilova,Korsakov,Dorogov,Shalygina

, p. 118 - 122 (2014)

Synthesis procedure of 3,5-dimethyl-4-heteryl-isoxazoles by reaction between heterocyclic aldehydes and nitroethane in the presence of base was developed. Sulfochlorination of the resulting compounds was studied.

Simple Synthesis of Symmetrical 4-Substituted 3,5-Dialkylisoxazoles

Best, Wayne M.,Ghisalberti, Emilio L.,Powell, Marianne

, p. 388 - 389 (2007/10/03)

A number of symmetrical 4-substituted 3,5-dialkylrsoxazoles have been prepared by treatment of aromatic aldehydes with nitroalkanes and aqueous sodium hydroxide.

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