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CAS

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148869-71-0

4-[N-acetyl-N-(4-nitrophenyl)amino]-4H-1,2,4-triazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 148869-71-0 Structure

  • Basic information

    1. Product Name: 4-[N-acetyl-N-(4-nitrophenyl)amino]-4H-1,2,4-triazole
    2. Synonyms: 4-[N-acetyl-N-(4-nitrophenyl)amino]-4H-1,2,4-triazole
    3. CAS NO:148869-71-0
    4. Molecular Formula:
    5. Molecular Weight: 247.213
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 148869-71-0.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-[N-acetyl-N-(4-nitrophenyl)amino]-4H-1,2,4-triazole(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-[N-acetyl-N-(4-nitrophenyl)amino]-4H-1,2,4-triazole(148869-71-0)
    11. EPA Substance Registry System: 4-[N-acetyl-N-(4-nitrophenyl)amino]-4H-1,2,4-triazole(148869-71-0)

  • 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: 148869-71-0(Hazardous Substances Data)

148869-71-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 148869-71-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,8,8,6 and 9 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 148869-71:
(8*1)+(7*4)+(6*8)+(5*8)+(4*6)+(3*9)+(2*7)+(1*1)=190
190 % 10 = 0
So 148869-71-0 is a valid CAS Registry Number.

148869-71-0Relevant articles and documents

Studies on aromatase inhibitors. I. Synthesis and biological evaluation of 4-amino-4H-1,2,4-triazole derivatives

Okada, Minoru,Yoden, Toru,Kawaminami, Eiji,Shimada, Yoshiaki,Kudoh, Masafumi,Isomura, Yasuo,Shikama, Hisataka,Fujikura, Takashi

, p. 1871 - 1879 (1996)

Various 4-N-substituted amino-4H-1,2,4-triazole derivatives were synthesized and evaluated for aromatase-inhibitory activity (in vitro) and for pregnant mare serum gonadotropin (PMSG)-induced estrogen synthesis- inhibitory activity (in vivo). The 4-(4-cya

Triazolylated teritiary amine compound or salt thereof

-

, (2008/06/13)

A triazolylated tertiary amine compound represented by general formula (I) or a salt thereof, having an aromatase inhibitory activity and being useful for preventing and treating breast cancer, mastopathy, endometriosis, prostatomergaly, etc., wherein A represents a single bond, lower alkylene or carbonyl; B represents lower alkyl, aryl, a 5- or 6-membered heterocyclic group, or a bicyclic fused heterocyclic group; D represents aryl, a 5- or 6-membered heterocyclic group, or a bicyclic fused heterocyclic group; and E represents 4H-1,2,4-triazolyl, 1H-1,2,4-triazolyl or 1H-1,2,3-triazolyl.

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