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1H-Benzimidazole-1-methanol,2-methyl-(9CI) is a chemical compound characterized by the molecular formula C9H10N2O. It is an organic compound within the benzimidazole class, which features a fused benzene and imidazole ring system. The specific 1-methanol, 2-methyl substitution on the benzimidazole ring endows 1H-Benzimidazole-1-methanol,2-methyl-(9CI) with distinctive properties, making it a versatile molecule for various applications, particularly in pharmaceuticals and organic synthesis. Due to potential health hazards, it is crucial to handle and regulate this chemical with care.

58566-85-1

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58566-85-1 Usage

Uses

Used in Pharmaceutical Industry:
1H-Benzimidazole-1-methanol,2-methyl-(9CI) is utilized as a pharmaceutical intermediate for the development of drugs targeting various therapeutic areas. Its unique structure allows for the creation of new drug candidates with potential applications in treating diseases and disorders.
Used in Organic Synthesis:
In the field of organic synthesis, 1H-Benzimidazole-1-methanol,2-methyl-(9CI) serves as a key building block for the synthesis of more complex organic molecules. Its reactivity and structural features make it a valuable component in the creation of novel compounds with diverse applications in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 58566-85-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,5,6 and 6 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 58566-85:
(7*5)+(6*8)+(5*5)+(4*6)+(3*6)+(2*8)+(1*5)=171
171 % 10 = 1
So 58566-85-1 is a valid CAS Registry Number.

58566-85-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-methylbenzimidazol-1-yl)methanol

1.2 Other means of identification

Product number -
Other names 1-Hydroxymethyl-2-methyl-benzimidazol

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:58566-85-1 SDS

58566-85-1Downstream Products

58566-85-1Relevant academic research and scientific papers

BENZIMIDAZOLYL COMPOUNDS AS POTENTIATORS OF MGLUR2 SUBTYPE OF GLUTAMATE RECEPTOR

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Page/Page column 56, (2010/11/30)

Compounds and pharmaceutically acceptable salts of the compounds are disclosed, wherein the compounds have the structure of Formula (I) as defined in the specification. Corresponding pharmaceutical compositions, methods of treatment, methods of synthesis, and intermediates are also disclosed.

BENZIMIDAZOLYL COMPOUNDS

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Page/Page column 70, (2010/11/29)

Compounds and pharmaceutically acceptable salts of the compounds are disclosed, wherein the compounds have the structure of formula (I) or pharmaceutically acceptable salts thereof, wherein Y1, R17, R2, R4, R5, R6, R7, R8, X2 and n are as defined in the detailed description of the invention. Corresponding pharmaceutical compositions, methods of treatment, methods of synthesis, and intermediates are also disclosed.

Application of ultrasound irradiation for the reactions of N-hydroxymethylation

Zhong,Song,Peng,Qian

, p. 3801 - 3807 (2007/10/03)

A convenient and high yield method for the N-hydroxymethylation of substituted phthalimide and benzimidazole under ultrasound irradiation is reported.

A SELECTIVE SYNTHESIS OF UNSYMMETRICAL 1,1'-METHYLENEBISDIAZOLES BY SOLID-LIQUID PHASE TRANSFER CATALYSIS

Julia, Sebastian,Martinez-Martorell, Carlos,Elguero, Jose

, p. 2233 - 2237 (2007/10/02)

1,1'-Methylenebisdiazoles Az1-CH2-Az2, Az1 and Az2 being two different diazoles, can be prepared selectively in three steps, through 1-hydroxymethyl- and 1-chloromethyldiazoles, by solid-liquid (S-L) phase transfer catalysis.

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