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N-benzyl-1-chloroisoquinoline-4-carboxamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1268691-29-7 Structure
  • Basic information

    1. Product Name: N-benzyl-1-chloroisoquinoline-4-carboxamide
    2. Synonyms: N-benzyl-1-chloroisoquinoline-4-carboxamide
    3. CAS NO:1268691-29-7
    4. Molecular Formula:
    5. Molecular Weight: 296.756
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1268691-29-7.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: N-benzyl-1-chloroisoquinoline-4-carboxamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-benzyl-1-chloroisoquinoline-4-carboxamide(1268691-29-7)
    11. EPA Substance Registry System: N-benzyl-1-chloroisoquinoline-4-carboxamide(1268691-29-7)
  • 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: 1268691-29-7(Hazardous Substances Data)

1268691-29-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1268691-29-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,8,6,9 and 1 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1268691-29:
(9*1)+(8*2)+(7*6)+(6*8)+(5*6)+(4*9)+(3*1)+(2*2)+(1*9)=197
197 % 10 = 7
So 1268691-29-7 is a valid CAS Registry Number.

1268691-29-7Upstream product

1268691-29-7Relevant articles and documents

Microwave-assisted synthesis of quinoline, isoquinoline, quinoxaline and quinazoline derivatives as CB2 receptor agonists

Saari, Raimo,T?rm?, Jonna-Carita,Nevalainen, Tapio

, p. 939 - 950 (2011)

Quinoline, isoquinoline, quinoxaline, and quinazoline derivatives were synthesized using microwave-assisted synthesis and their CB1/CB2 receptor activities were determined using the [35S]GTPγS binding assay. Most of the prepared quinoline, isoquinoline, and quinoxalinyl phenyl amines showed low-potency partial CB2 receptor agonists activity. The most potent CB2 ligand was the 4-morpholinylmethanone derivative (compound 40e) (-log EC 50 = 7.8; Emax = 75%). The isoquinolin-1-yl(3- trifluoromethyl-phenyl)amine (compound 26c) was a high efficacy CB2 agonist (-log EC50 = 5.8; Emax = 128%). No significant CB1 receptor activation or inactivation was shown in these studies, except 40e, which showed weak CB1 agonist activity (CB1 -log EC50 = 5.0). These ligands serve as novel templates for the development of selective CB2 receptor agonist.

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