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CAS

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1450981-15-3

4-ethyl 2,2-dimethyl 5-methyl-3-[methyl(phenyl)amino]furan-2,2,4(3H)-tricarboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1450981-15-3 Structure

  • Basic information

    1. Product Name: 4-ethyl 2,2-dimethyl 5-methyl-3-[methyl(phenyl)amino]furan-2,2,4(3H)-tricarboxylate
    2. Synonyms:
    3. CAS NO:1450981-15-3
    4. Molecular Formula:
    5. Molecular Weight: 377.394
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1450981-15-3.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: 4-ethyl 2,2-dimethyl 5-methyl-3-[methyl(phenyl)amino]furan-2,2,4(3H)-tricarboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-ethyl 2,2-dimethyl 5-methyl-3-[methyl(phenyl)amino]furan-2,2,4(3H)-tricarboxylate(1450981-15-3)
    11. EPA Substance Registry System: 4-ethyl 2,2-dimethyl 5-methyl-3-[methyl(phenyl)amino]furan-2,2,4(3H)-tricarboxylate(1450981-15-3)

  • 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: 1450981-15-3(Hazardous Substances Data)

1450981-15-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1450981-15-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,5,0,9,8 and 1 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1450981-15:
(9*1)+(8*4)+(7*5)+(6*0)+(5*9)+(4*8)+(3*1)+(2*1)+(1*5)=163
163 % 10 = 3
So 1450981-15-3 is a valid CAS Registry Number.

1450981-15-3Downstream Products

1450981-15-3Relevant articles and documents

Reactions of enaminones with diazocarbonyl compounds

Güng?r, Füsun ?eyma,Hancio?lu, Neslihan,Ana?, Olcay

, p. 488 - 493 (2013)

The [Cu(acac)2]-catalyzed reactions of several tertiary enaminones with three diazocarbonyl compounds, i.e., dimethyl diazomalonate, ethyl diazoacetoacetate, and ethyl diazoacetate, yielded amino- and additionally carbonyl-substituted dihydrofurans, together with further furan derivatives. Due to the conjugation of α-carbonyl/α-Ph groups, reactions proceeded only via 1,5-electrocyclization of corresponding keto-ylides. On the other hand, in the absence of any α-substituent, tertiary enaminone and ethyl diazoacetate, reacted via an accompanying mechanism by a push-pull cyclopropane intermediate, to yield a 2,4-dicarbonyl-substituted furan in one step with moderate yield. Copyright

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