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6-Methyl-1H-benzoimidazole-2-carbaldehyde is a chemical compound characterized by the molecular formula C9H8N2O. It is a yellowish solid that plays a significant role in the field of organic synthesis, particularly in the creation of pharmaceuticals and other compounds. This versatile chemical serves as a building block for pharmaceuticals, an intermediate in chemical reactions, and a research compound for studying the properties and behaviors of different chemical structures. Due to its potential hazards when ingested, inhaled, or comes into contact with the skin or eyes, careful handling is essential.

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  • 883541-93-3 Structure
  • Basic information

    1. Product Name: 6-METHYL-1H-BENZOIMIDAZOLE-2-CARBALDEHYDE
    2. Synonyms: 6-METHYL-1H-BENZOIMIDAZOLE-2-CARBALDEHYDE;6-methyl-1H-Benzimidazole-2-carboxaldehyde;5-Methyl-1H-benzoimidazole-2-carbaldehyde
    3. CAS NO:883541-93-3
    4. Molecular Formula: C9H8N2O
    5. Molecular Weight: 160.17
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 883541-93-3.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.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 6-METHYL-1H-BENZOIMIDAZOLE-2-CARBALDEHYDE(CAS DataBase Reference)
    10. NIST Chemistry Reference: 6-METHYL-1H-BENZOIMIDAZOLE-2-CARBALDEHYDE(883541-93-3)
    11. EPA Substance Registry System: 6-METHYL-1H-BENZOIMIDAZOLE-2-CARBALDEHYDE(883541-93-3)
  • 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: 883541-93-3(Hazardous Substances Data)

883541-93-3 Usage

Uses

Used in Pharmaceutical Industry:
6-Methyl-1H-benzoimidazole-2-carbaldehyde is used as a building block for the synthesis of various pharmaceuticals, contributing to the development of new drugs and therapeutic agents. Its unique chemical structure allows for the creation of a wide range of compounds with potential medicinal properties.
Used in Chemical Reactions:
As an intermediate in chemical reactions, 6-Methyl-1H-benzoimidazole-2-carbaldehyde facilitates the synthesis of complex organic compounds. Its presence in these reactions enables the formation of desired products, making it a valuable component in the process of organic synthesis.
Used in Research and Development:
6-Methyl-1H-benzoimidazole-2-carbaldehyde is utilized as a research compound for studying the properties and behaviors of different chemical structures. Its unique characteristics provide valuable insights into the field of organic chemistry, aiding in the understanding of molecular interactions and the development of novel synthetic pathways.

Check Digit Verification of cas no

The CAS Registry Mumber 883541-93-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,3,5,4 and 1 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 883541-93:
(8*8)+(7*8)+(6*3)+(5*5)+(4*4)+(3*1)+(2*9)+(1*3)=203
203 % 10 = 3
So 883541-93-3 is a valid CAS Registry Number.

883541-93-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-methyl-1H-benzimidazole-2-carbaldehyde

1.2 Other means of identification

Product number -
Other names 6-METHYL-1H-BENZO[D]IMIDAZOLE-2-CARBALDEHYDE

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:883541-93-3 SDS

883541-93-3Downstream Products

883541-93-3Relevant articles and documents

PYRAZOLOPYRAZINES ACTING ON CANCERS VIA INHIBITION OF CDK12

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Page/Page column 155, (2021/09/11)

The present invention provides compounds of general formula (I) in which X, R1, R2 and R3 are as described and defined herein, methods of preparing said compounds, intermediate compounds useful for preparing said compounds, pharmaceutical compositions and combinations comprising said compounds, and the use of said compounds for manufacturing pharmaceutical compositions for the treatment and/or prophylaxis of diseases, in particular of hyperproliferative disorders such as cancer disorders, as a sole agent or in combination with other active ingredients.

One-Pot Base-Mediated Synthesis of Functionalized Aza-Fused Polycyclic Quinoline Derivatives

Jiang, Zeng-Qiang,Miao, Da-Zhuang,Tong, Yao,Pan, Qiang,Li, Xiao-Tong,Hu, Ren-He,Han, Shi-Qing

supporting information, p. 1913 - 1921 (2015/06/30)

A new one-pot protocol has been developed for the facile and efficient synthesis of aza-fused polycyclic quinolines (e.g., pyrrolo[1,2-a]quinolines) by the base-catalyzed reaction of 2-formylpyrroles and 2-halophenylacetonitriles. This reaction proceeded under transition metal-free conditions and showed high functional group tolerance, with the desired products being formed in good yields.

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