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2-BUTYL-5,6-DICHLORO-1H-1,3-BENZIMIDAZOLE is a chemical compound belonging to the benzimidazole class, characterized by the molecular formula C11H10Cl2N2 and a molecular weight of 235.12 g/mol. This derivative features two chlorine atoms and a butyl group, which contribute to its unique chemical properties and potential applications in various fields.

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  • 133052-59-2 Structure
  • Basic information

    1. Product Name: 2-BUTYL-5,6-DICHLORO-1H-1,3-BENZIMIDAZOLE
    2. Synonyms: 2-Butyl-5,6-dichloro-1H-benzo[d]iMidazole;2-Butyl-5,6-dichloro-1H-benzimidazole;2-BUTYL-5,6-DICHLORO-1H-1,3-BENZIMIDAZOLE
    3. CAS NO:133052-59-2
    4. Molecular Formula: C11H12Cl2N2
    5. Molecular Weight: 243.13
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 133052-59-2.mol
  • Chemical Properties

    1. Melting Point: 149-151°
    2. Boiling Point: 423°Cat760mmHg
    3. Flash Point: 242.2°C
    4. Appearance: /
    5. Density: 1.315g/cm3
    6. Vapor Pressure: 5.68E-07mmHg at 25°C
    7. Refractive Index: 1.623
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 2-BUTYL-5,6-DICHLORO-1H-1,3-BENZIMIDAZOLE(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2-BUTYL-5,6-DICHLORO-1H-1,3-BENZIMIDAZOLE(133052-59-2)
    12. EPA Substance Registry System: 2-BUTYL-5,6-DICHLORO-1H-1,3-BENZIMIDAZOLE(133052-59-2)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: IRRITANT
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 133052-59-2(Hazardous Substances Data)

133052-59-2 Usage

Uses

Used in Pharmaceutical Synthesis:
2-BUTYL-5,6-DICHLORO-1H-1,3-BENZIMIDAZOLE is utilized as a key intermediate in the synthesis of pharmaceuticals, particularly for the development of antiparasitic and anticancer drugs. Its unique structure allows for the creation of novel therapeutic agents with enhanced efficacy and selectivity.
Used in Research and Development:
As a research chemical, 2-BUTYL-5,6-DICHLORO-1H-1,3-BENZIMIDAZOLE is employed in the study of benzimidazole derivatives and their potential biological activities. This helps researchers to better understand the structure-activity relationships and discover new applications for these compounds.
Used in Anti-inflammatory and Analgesic Applications:
Due to its reported anti-inflammatory and analgesic properties, 2-BUTYL-5,6-DICHLORO-1H-1,3-BENZIMIDAZOLE has potential use in the treatment of various medical conditions, such as pain and inflammation. Its incorporation into pharmaceutical formulations could provide relief for patients suffering from these conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 133052-59-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,0,5 and 2 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 133052-59:
(8*1)+(7*3)+(6*3)+(5*0)+(4*5)+(3*2)+(2*5)+(1*9)=92
92 % 10 = 2
So 133052-59-2 is a valid CAS Registry Number.
InChI:InChI=1/C11H12Cl2N2/c1-2-3-4-11-14-9-5-7(12)8(13)6-10(9)15-11/h5-6H,2-4H2,1H3,(H,14,15)

133052-59-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-butyl-5,6-dichloro-1H-benzimidazole

1.2 Other means of identification

Product number -
Other names 2-butyl-5,6-dichlorobenzimidazole

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:133052-59-2 SDS

133052-59-2Relevant articles and documents

Substituted benzimidazoles as angiotensin II antagonists

-

, (2008/06/13)

There are disclosed new substituted benzimidazole compounds and derivatives thereof which are useful as angiotensin II antagonists. These compounds have the general formula:

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