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40132-09-0

3-benzyl-1,2,3,4-tetrahydro-quinazoline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 40132-09-0 Structure

  • Basic information

    1. Product Name: 3-benzyl-1,2,3,4-tetrahydro-quinazoline
    2. Synonyms: 3-benzyl-1,2,3,4-tetrahydro-quinazoline
    3. CAS NO:40132-09-0
    4. Molecular Formula:
    5. Molecular Weight: 224.305
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 40132-09-0.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: 3-benzyl-1,2,3,4-tetrahydro-quinazoline(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-benzyl-1,2,3,4-tetrahydro-quinazoline(40132-09-0)
    11. EPA Substance Registry System: 3-benzyl-1,2,3,4-tetrahydro-quinazoline(40132-09-0)

  • 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: 40132-09-0(Hazardous Substances Data)

40132-09-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 40132-09-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,1,3 and 2 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 40132-09:
(7*4)+(6*0)+(5*1)+(4*3)+(3*2)+(2*0)+(1*9)=60
60 % 10 = 0
So 40132-09-0 is a valid CAS Registry Number.

40132-09-0Downstream Products

40132-09-0Relevant articles and documents

The development of carbon-carbon bond forming reactions of aminal radicals

Schiedler, David A.,Vellucci, Jessica K.,Lu, Yi,Beaudry, Christopher M.

, p. 1448 - 1465 (2015/02/19)

Aminal radicals were generated and used in synthetic reactions for the first time. Aminal radicals are formed from aminals by radical translocation using AIBN and a stoichiometric hydrogen atom donor, or by SmI2 reduction of N-acyl amidines or amidinium ions in the presence of a proton source. Aminal radicals were found to participate in inter- and intramolecular C-C bond forming reactions with electron deficient alkenes. Chemical yields were as high as 99%.

Formation of carbon-carbon bonds using aminal radicals

Schiedler, David A.,Vellucci, Jessica K.,Beaudry, Christopher M.

, p. 6092 - 6095 (2013/02/23)

Aminal radicals were generated by radical translocation processes. For the first time, it is shown that they participate in carbon-carbon bond forming reactions. Either stannane or silane hydrogen atom donors are suitable for the reaction. More than 30 su

Synthesis and in vitro study of platelet antiaggregant activity of 1,2,3,4-tetrahydroquinazoline derivatives

Gravier,Dupin,Casadebaig,Hou,Boisseau,Bernard

, p. 531 - 535 (2007/10/02)

Some original 3-substituted 1,2,3,4-tetrahydroquinazolines were synthesized. Their antiplatelet activity was evaluated in vitro with respect to aggregation induced by the main inducers (ADP, collagen, arachidonic acid), platelet serotonin release reaction and thromboxane A2 synthesis. All these molecules possess an inhibiting power which, compared to that of aspirin in the same conditions, is the same or greater when aggregation is induced by ADP.

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