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CAS

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1083067-78-0

4-(4-ethoxyphenyl)-1-[(1,2,4-triazol-1-yl)acetyl]semicarbazide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1083067-78-0 Structure

  • Basic information

    1. Product Name: 4-(4-ethoxyphenyl)-1-[(1,2,4-triazol-1-yl)acetyl]semicarbazide
    2. Synonyms:
    3. CAS NO:1083067-78-0
    4. Molecular Formula:
    5. Molecular Weight: 304.308
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1083067-78-0.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: 4-(4-ethoxyphenyl)-1-[(1,2,4-triazol-1-yl)acetyl]semicarbazide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-(4-ethoxyphenyl)-1-[(1,2,4-triazol-1-yl)acetyl]semicarbazide(1083067-78-0)
    11. EPA Substance Registry System: 4-(4-ethoxyphenyl)-1-[(1,2,4-triazol-1-yl)acetyl]semicarbazide(1083067-78-0)

  • 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: 1083067-78-0(Hazardous Substances Data)

1083067-78-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1083067-78-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,8,3,0,6 and 7 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1083067-78:
(9*1)+(8*0)+(7*8)+(6*3)+(5*0)+(4*6)+(3*7)+(2*7)+(1*8)=150
150 % 10 = 0
So 1083067-78-0 is a valid CAS Registry Number.

1083067-78-0Relevant articles and documents

Synthesis and structure of mono- and disubstituted derivatives of 4,5-dihydro-1H-1,2,4-triazol-5-one

Pitucha,Dobosz,Stepniak,Dybala,Koziol

, p. 2103 - 2114 (2008/09/18)

In the reaction of hydrazide of 1,2,4-triazol-1-acetic acid with isocyanates the semi-carbazide derivatives were obtained (Ia-Ii). Depending on the chemical nature of the starting isocyanate, cyclization of Ia-Ii in alkaline medium led to formation of three groups of derivatives of 4,5-dihydro-1H-1,2,4- triazol-5-one (IIa-IIi). Alkyl and aryl substituents of semicarbazides formed 3,4-disubstituted compounds (IIa-IIf), the ethoxycarbonyl group promoted formation of 3-substituted compound IIg, while compounds IIh and IIi are 4-substituted triazol-5-ones resulting from benzoyl and benzenesulfonyl isocyanates. Molecular structures of three products (IIb, IIc, IId) were confirmed by the X-ray structure analysis. Different substituents at the N4 atom (ethyl in IIb, cyclohexyl in IIc and 1-naphthyl in IId) influence the molecular association pattern in the crystal structure.

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