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CAS

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141034-99-3

1H-Pyrazole-4,5-dicarboxylic acid, 4-(acetylamino)-4,5-dihydro-3-phenyl-, dimethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 141034-99-3 Structure

  • Basic information

    1. Product Name: 1H-Pyrazole-4,5-dicarboxylic acid, 4-(acetylamino)-4,5-dihydro-3-phenyl-, dimethyl ester
    2. Synonyms:
    3. CAS NO:141034-99-3
    4. Molecular Formula: C15H17N3O5
    5. Molecular Weight: 319.317
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 141034-99-3.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: 1H-Pyrazole-4,5-dicarboxylic acid, 4-(acetylamino)-4,5-dihydro-3-phenyl-, dimethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1H-Pyrazole-4,5-dicarboxylic acid, 4-(acetylamino)-4,5-dihydro-3-phenyl-, dimethyl ester(141034-99-3)
    11. EPA Substance Registry System: 1H-Pyrazole-4,5-dicarboxylic acid, 4-(acetylamino)-4,5-dihydro-3-phenyl-, dimethyl ester(141034-99-3)

  • 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: 141034-99-3(Hazardous Substances Data)

141034-99-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 141034-99-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,0,3 and 4 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 141034-99:
(8*1)+(7*4)+(6*1)+(5*0)+(4*3)+(3*4)+(2*9)+(1*9)=93
93 % 10 = 3
So 141034-99-3 is a valid CAS Registry Number.

141034-99-3Downstream Products

141034-99-3Relevant articles and documents

Synthesis of cyclopropane derivatives of aspartic acid by thermal decomposition of substituted pyrazolines

Anisimova,Berkova,Paperno,Deiko

, p. 460 - 463 (2002)

Thermal decomposition of substituted Δ1- and Δ 2-pyrazolines was used to obtain cyclopropane derivatives of aspartic and adipic acids.

Catalytic cyclopropanation of alkyl 2-allyl-2-acetylaminomalonate and methyl N-(acetyl)(phenyl)dehydroalanine with alkyl diazoacetates

Anisimova,Berkova,Paperno,Deiko

, p. 272 - 275 (2002)

Cyclopropane analogs of aspartic and adipic acids were prepared by catalytic cyclopropanation of dehydro amino acid derivatives with alkyl diazoacetates in the presence of catalyst (dirhodium tetraacetate).

Synthesis of 5-acetylaimno-3,5-dialkoxycarbonyl-and 4-acetylamino-4,5-dialkoxycarbonyl-3-phenyl-Δ2-pyrazolines

Anisimova,Berkova,Deiko,Pozdnyakov

, p. 1469 - 1472 (2007/10/03)

1,3-Dipolar cycloaddition of alkyl diazoacetates to methyl N-acetylaminoalkenoates leads to pyrazoline and cyclopropane derivatives in a ratio depending on the polarity of the solvent.

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