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5,6-Dimethoxybenzimidazole, with the chemical formula C9H10N2O2 and CAS number 56205-66-6, is an organic compound that appears as an off-white crystalline powder. It is moderately soluble in water and is known for its biological activities, which make it a valuable intermediate in the pharmaceutical industry.

72721-02-9

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72721-02-9 Usage

Uses

Used in Pharmaceutical Industry:
5,6-Dimethoxybenzimidazole is used as a key intermediate in the synthesis of various drugs, contributing to their development and effectiveness in treating different medical conditions. Its specific chemical structure allows for the creation of new drug molecules with potential therapeutic benefits.
Safety Considerations:
While 5,6-Dimethoxybenzimidazole is a useful compound in pharmaceutical applications, it is important to handle it with care due to its potential to cause eye or skin irritation. Additionally, it may have harmful effects if absorbed into the body, so appropriate protective measures should be taken during its use and production.

Check Digit Verification of cas no

The CAS Registry Mumber 72721-02-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,7,2 and 1 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 72721-02:
(7*7)+(6*2)+(5*7)+(4*2)+(3*1)+(2*0)+(1*2)=109
109 % 10 = 9
So 72721-02-9 is a valid CAS Registry Number.

72721-02-9 Well-known Company Product Price

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  • Alfa Aesar

  • (H25942)  5,6-Dimethoxybenzimidazole, 98%   

  • 72721-02-9

  • 1g

  • 2856.0CNY

  • Detail
  • Alfa Aesar

  • (H25942)  5,6-Dimethoxybenzimidazole, 98%   

  • 72721-02-9

  • 5g

  • 10388.0CNY

  • Detail

72721-02-9SDS

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 5,6-dimethoxy-1H-benzimidazole

1.2 Other means of identification

Product number -
Other names 5,6-dimethoxy-1H-benzo[d]imidazole

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:72721-02-9 SDS

72721-02-9Relevant articles and documents

Efficient N-Heterocyclic Carbene/Ruthenium Catalytic Systems for the Alcohol Amidation with Amines: Involvement of Poly-Carbene Complexes?

Cheng, Hua,Xiong, Mao-Qian,Zhang, Ni,Wang, Hua-Jing,Miao, Yang,Su, Wei,Yuan, Ye,Chen, Cheng,Verpoort, Francis

, p. 4338 - 4345 (2018/09/06)

The atom-economic direct amidation of alcohols with amines has been recently highlighted as an attractive and promising transformation. Among the versatile reported catalytic systems, in situ generated N-heterocyclic carbene (NHC)/ruthenium (Ru) catalytic systems have demonstrated their advantages such as easy operation and use of commercial Ru compounds. However, the existing catalyst loadings are relatively high, and additional insights for the in situ catalyst generation are still not well-documented. In this work, a variety of benzimidazole-based NHC precursors were initially synthesized. Through the screening of various NHC precursors and other reaction conditions, active in situ catalytic systems were discovered for the efficient amide synthesis. Notably, the catalyst loading is as low as 0.5 mol %. Furthermore, additional experiments were performed to validate the rationale for the superiority of the current catalytic systems over our previous system. It was observed that the ligand structure is one of the reasons for the higher activity. In addition, the higher ratio of the NHC precursor/[Ru] is another important factor for the improvement. Further HR-MS analysis identified the formation of two mono-NHC-Ru species as major species and two Ru species bearing multiple NHC ligands as minor species. Hopefully, the efficient and readily-accessible catalytic systems reported herein could demonstrate great potential for further practical applications.

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

7-Substituted Purine Derivatives for Immunosuppression

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Page/Page column 9, (2008/12/05)

The present invention provides novel purinone and related derivatives useful for the prevention and treatment of autoimmune diseases, inflammatory disease, mast cell mediated disease and transplant rejection. The compounds are of the general formula III:

7-SUBSTITUTED PURINE DERIVATIVES FOR IMMUNOSUPPRESSION

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Page/Page column 28, (2008/12/05)

The present invention provides novel purinone and related derivatives useful for the prevention and treatment of autoimmune diseases, inflammatory disease, mast cell mediated disease and transplant rejection. The compounds are of the general formula (III).

Thiazolyl-benzimidazoles

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Page/Page column 41, (2008/06/13)

The invention is directed to compounds of formula (1) [image] and pharmaceutically acceptable salts thereof, methods for the preparation thereof, and methods of use thereof.

PURINE AND IMIDAZOPYRIDINE DERIVATIVES FOR IMMUNOSUPPRESSION

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Page/Page column 29, (2010/11/24)

The present invention provides novel purine and imidazopyridine derivatives useful for the prevention and treatment of autoimmune diseases, inflammatory disease, mast cell mediated disease and transplant rejection. The compounds are of the general formulas ( I ) and ( II ).

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