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4-(2-chloro-4-bromophenyl)amine-6,7,8-trimethoxyquinazoline hydrochloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 949920-92-7 Structure
  • Basic information

    1. Product Name: 4-(2-chloro-4-bromophenyl)amine-6,7,8-trimethoxyquinazoline hydrochloride
    2. Synonyms: 4-(2-chloro-4-bromophenyl)amine-6,7,8-trimethoxyquinazoline hydrochloride
    3. CAS NO:949920-92-7
    4. Molecular Formula:
    5. Molecular Weight: 461.142
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 949920-92-7.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-(2-chloro-4-bromophenyl)amine-6,7,8-trimethoxyquinazoline hydrochloride(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-(2-chloro-4-bromophenyl)amine-6,7,8-trimethoxyquinazoline hydrochloride(949920-92-7)
    11. EPA Substance Registry System: 4-(2-chloro-4-bromophenyl)amine-6,7,8-trimethoxyquinazoline hydrochloride(949920-92-7)
  • 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: 949920-92-7(Hazardous Substances Data)

949920-92-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 949920-92-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,9,9,2 and 0 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 949920-92:
(8*9)+(7*4)+(6*9)+(5*9)+(4*2)+(3*0)+(2*9)+(1*2)=227
227 % 10 = 7
So 949920-92-7 is a valid CAS Registry Number.

949920-92-7Downstream Products

949920-92-7Relevant articles and documents

Synthesis and biological activity of novel N-substituted 4-amino-6,7,8-trimethoxyquinazoline compounds

Liu, Gang,Liu, Chunping,Sun, Lin,Qu, Rongjun,Chen, Hou,Ji, Chunnuan

, p. 1290 - 1300 (2007)

A series of N-substituted 4-amino-6,7,8-trimethoxyquinazoline derivatives has been synthesized from 4-chloro-6,7,8-trimethoxyquinazoline and aryl (or benzyl) amines using 2-propanol as a solvent. The starting material 4-chloro-6,7,8-trimethoxyquinazoline has been synthesized from natural gallic acid by a novel route. Their structures have been verified by elemental analysis and IR, 1H, and 13C NMR spectroscopy. The title compounds have been evaluated for their in vitro antiproliferative activities against some cancer cells by the MTT method. Unfortunately, most of the compounds tested have exhibited a weaker anticancer activity than the reference standard drug PD153035.

Microwave assisted synthesis of novel 6,7,8-trimethoxy N-substituted-4- aminoquinazoline compounds

Liu, Gang,Sun, Lin,Liu, Chunping,Ji, Chunnuan,Wen, Quanwu,Ma, Songmei

, p. 759 - 764 (2008/09/21)

(Chemical Equation Presented) A fast, efficient and convenient reaction of 6,7,8-trimethoxy-4-chloroquinazoline and aryl (or benzyl) amines was achieved under microwave irradiation in isopropyl alcohol, providing a simple method for synthesis of novel 6,7,8-trimethoxy N-substituted-4-aminoquinazoline compounds in good yield in short time. The title compounds were evaluated for their in vitro anti-proliferative activities against PC3 cell by MTT method.

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