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2-Methyl-5,6-dimethoxybenzimidazole, a benzimidazole derivative with the molecular formula C10H12N2O2, is a heterocyclic organic compound that serves as a versatile building block in the synthesis of pharmaceuticals and agrochemicals. Its potential anti-inflammatory and anti-cancer properties, along with its application as a corrosion inhibitor in metal protection, make it a compound of interest in various scientific and industrial fields.

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  • 51437-32-2 Structure
  • Basic information

    1. Product Name: 2-METHYL-5,6-DIMETHOXYBENZIMIDAZOLE
    2. Synonyms: 2-METHYL-5,6-DIMETHOXYBENZIMIDAZOLE;5,6-Dimethoxy-2-methylbenzimidazole;1H-Benzimidazole,5,6-dimethoxy-2-methyl-(9CI)
    3. CAS NO:51437-32-2
    4. Molecular Formula: C10H12N2O2
    5. Molecular Weight: 192.21
    6. EINECS: N/A
    7. Product Categories: BENZIMIDAZOLE;Imidazol&Benzimidazole
    8. Mol File: 51437-32-2.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 390.5 °C at 760 mmHg
    3. Flash Point: 141.8 °C
    4. Appearance: /
    5. Density: 1.206 g/cm3
    6. Vapor Pressure: 5.94E-06mmHg at 25°C
    7. Refractive Index: 1.603
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 2-METHYL-5,6-DIMETHOXYBENZIMIDAZOLE(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2-METHYL-5,6-DIMETHOXYBENZIMIDAZOLE(51437-32-2)
    12. EPA Substance Registry System: 2-METHYL-5,6-DIMETHOXYBENZIMIDAZOLE(51437-32-2)
  • 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: 51437-32-2(Hazardous Substances Data)

51437-32-2 Usage

Uses

Used in Pharmaceutical and Agrochemical Industries:
2-Methyl-5,6-dimethoxybenzimidazole is used as a key intermediate in the synthesis of various pharmaceuticals and agrochemicals for its ability to contribute to the development of new drugs and pesticides.
Used in Anti-inflammatory and Anti-cancer Applications:
2-Methyl-5,6-dimethoxybenzimidazole is used as a potential therapeutic agent for its anti-inflammatory and anti-cancer properties, offering a promising avenue for the treatment of various inflammatory and neoplastic conditions.
Used in Metal Protection Industry:
2-Methyl-5,6-dimethoxybenzimidazole is used as a corrosion inhibitor in metal protection, providing a means to prevent the degradation of metal surfaces and extend the lifespan of metal structures and components.
Safety Considerations:
It is important to handle 2-Methyl-5,6-dimethoxybenzimidazole with care, as exposure to high concentrations can cause irritation to the skin, eyes, and respiratory system, necessitating proper safety measures during its use and manipulation.

Check Digit Verification of cas no

The CAS Registry Mumber 51437-32-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,4,3 and 7 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 51437-32:
(7*5)+(6*1)+(5*4)+(4*3)+(3*7)+(2*3)+(1*2)=102
102 % 10 = 2
So 51437-32-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H12N2O2/c1-6-11-7-4-9(13-2)10(14-3)5-8(7)12-6/h4-5H,1-3H3,(H,11,12)

51437-32-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 5,6-dimethoxy-2-methyl-1H-benzimidazole

1.2 Other means of identification

Product number -
Other names HMS1581I05

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:51437-32-2 SDS

51437-32-2Relevant articles and documents

Expanding the aqueous-based redox-facilitated self-polymerization chemistry of catecholamines to 5,6-dihydroxy-1H-benzimidazole and its 2-substituted derivatives

Fan, Ka Wai,Peterson, Matthew B.,Ellersdorfer, Peter,Granville, Anthony M.

, p. 25203 - 25214 (2016/03/22)

Aqueous-base redox-facilitated self-polymerization can be performed with 5,6-dihydroxy-1H-benzimidazole (DHBI) to generate polymeric material that is analogous to poly(dopamine) (PDA), proving the possibility to expand the catecholamine-exclusive chemistr

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