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  • 188860-26-6 Structure
  • Basic information

    1. Product Name: DMA
    2. Synonyms: 2,5'-Bi-1H-benzimidazole, 2'-(3,4-dimethoxyphenyl)-5-(4-methyl-1-piperazinyl)-;2'-(3,4-Dimethoxyphenyl)-5-(4-methylpiperazin-1-yl)-1H,1'H-2,5'-bibenzo[d]imidazole
    3. CAS NO:188860-26-6
    4. Molecular Formula: C27H28N6O2
    5. Molecular Weight: 468.55022
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 188860-26-6.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: 2-8°C
    8. Solubility: N/A
    9. CAS DataBase Reference: DMA(CAS DataBase Reference)
    10. NIST Chemistry Reference: DMA(188860-26-6)
    11. EPA Substance Registry System: DMA(188860-26-6)
  • 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: 188860-26-6(Hazardous Substances Data)

188860-26-6 Usage

Benzimidazole derivative

Contains a benzimidazole core, which is a key structural component in this compound.

Substituted phenyl and piperazine groups

The benzimidazole core is connected to a 3,4-dimethoxyphenyl group (a phenyl group with methoxy substituents at the 3 and 4 positions) and a 6-(4-methylpiperazin-1-yl) group (a piperazine group with a methyl substituent).

Potential biological activity

The compound is being studied for its possible biological effects and interactions.

Pharmaceutical agent potential

Researchers are exploring the possibility of using this compound as a pharmaceutical agent due to its potential biological activity.

Central nervous system functions

The compound may have functions related to the central nervous system, indicating a potential role in modulating neural processes.

Receptor ligand for neurotransmitter systems

The structure of the compound suggests that it may act as a receptor ligand, binding to specific receptors in neurotransmitter systems and influencing their activity.

Further research needed

More research is required to fully understand the properties, potential applications, and mechanisms of action of this complex organic compound.

Check Digit Verification of cas no

The CAS Registry Mumber 188860-26-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,8,8,6 and 0 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 188860-26:
(8*1)+(7*8)+(6*8)+(5*8)+(4*6)+(3*0)+(2*2)+(1*6)=186
186 % 10 = 6
So 188860-26-6 is a valid CAS Registry Number.

188860-26-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(3,4-dimethoxyphenyl)-6-[6-(4-methylpiperazin-1-yl)-1H-benzimidazol-2-yl]-1H-benzimidazole

1.2 Other means of identification

Product number -
Other names DMA|

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:188860-26-6 SDS

188860-26-6Downstream Products

188860-26-6Relevant articles and documents

Synthesis and biological activity of novel inhibitors of topoisomerase I: 2-Aryl-substituted 2-bis-1H-benzimidazoles

Singh, Manish,Tandon, Vibha

, p. 659 - 669 (2011/03/19)

Inhibitors of topoisomerase I constitute a novel family of antitumor agents. The class of benzimidazole derivatives contains compounds possessing affinity to DNA. For example, fluorescent stains Hoechst 33342 and Hoechst 33258 interact with DNA as ligand

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