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6,8-dibromo-N2,N4-bis(3-chlorophenyl)quinazoline-2,4-diamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1629730-59-1 Structure
  • Basic information

    1. Product Name: 6,8-dibromo-N2,N4-bis(3-chlorophenyl)quinazoline-2,4-diamine
    2. Synonyms: 6,8-dibromo-N2,N4-bis(3-chlorophenyl)quinazoline-2,4-diamine
    3. CAS NO:1629730-59-1
    4. Molecular Formula:
    5. Molecular Weight: 539.056
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1629730-59-1.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: 6,8-dibromo-N2,N4-bis(3-chlorophenyl)quinazoline-2,4-diamine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 6,8-dibromo-N2,N4-bis(3-chlorophenyl)quinazoline-2,4-diamine(1629730-59-1)
    11. EPA Substance Registry System: 6,8-dibromo-N2,N4-bis(3-chlorophenyl)quinazoline-2,4-diamine(1629730-59-1)
  • 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: 1629730-59-1(Hazardous Substances Data)

1629730-59-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1629730-59-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,2,9,7,3 and 0 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1629730-59:
(9*1)+(8*6)+(7*2)+(6*9)+(5*7)+(4*3)+(3*0)+(2*5)+(1*9)=191
191 % 10 = 1
So 1629730-59-1 is a valid CAS Registry Number.

1629730-59-1Downstream Products

1629730-59-1Relevant articles and documents

Efficient access to 2,6,8-trisubstituted 4-aminoquinazolines through microwave-assisted one-pot chemoselective Tris-Suzuki-Miyaura or SNAr/bis-Suzuki-Miyaura reactions in water

Kabri, Youssef,Crozet, Maxime D.,Terme, Thierry,Vanelle, Patrice

, p. 3806 - 3817 (2015)

An efficient, sequential, one-pot strategy for synthesizing polyfunctionalized quinazoline derivatives is presented. After selective amination of 6,8-dibromo-2,4-dichloroquinazoline at the C-4 position, 2,6,8-trisubstituted 4-aminoquinazoline derivatives

One-pot chemoselective synthesis of 2,4,6,8-tetrasubstituted quinazolines via microwave-assisted consecutive bis-SNAr/Bis-Suzuki-Miyaura cross-coupling reactions

Kabri, Youssef,Crozet, Maxime D.,Redon, Sebastien,Vanelle, Patrice

, p. 1613 - 1620 (2014/06/23)

A practical and efficient synthesis of 2,4,6,8-tetrasubstituted quinazolines through one-pot chemoselective sequential bis-SNAr/bis- Suzuki-Miyaura reactions under microwave irradiation is presented. The bis-SNAr reaction occurs selectively at the C-2 and C-4 positions of 6,8-dibromo-2,4-dichloroquinazoline and the bis-Suzuki-Miyaura cross-coupling at C-6 and C-8. This procedure affords convergent synthesis of polysubstituted quinazoline derivatives in high yields in very few steps and tolerates a wide range of boronic acids and amines.

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