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13109-82-5

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13109-82-5 Usage

General Description

1H-Benzimidazole, 2-(diethoxymethyl)-, commonly known as DEBIO-025, is a chemical compound composed of a benzimidazole ring and a diethoxymethyl side chain. It has been studied for its potential antiviral and antifungal properties, and has shown promise as a treatment for hepatitis C and other viral infections. DEBIO-025 has been shown to inhibit the replication of the hepatitis C virus by blocking the action of the viral protein cyclophilin A. It has also been investigated for its potential as an antifungal agent, with studies demonstrating its effectiveness against various fungal species. Additionally, DEBIO-025 has been explored for its potential use in cancer therapy, due to its ability to inhibit the proliferation of cancer cells. Overall, DEBIO-025 shows potential as a versatile compound with promising applications in the fields of antiviral, antifungal, and cancer treatment.

Check Digit Verification of cas no

The CAS Registry Mumber 13109-82-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,1,0 and 9 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 13109-82:
(7*1)+(6*3)+(5*1)+(4*0)+(3*9)+(2*8)+(1*2)=75
75 % 10 = 5
So 13109-82-5 is a valid CAS Registry Number.

13109-82-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(Diethoxymethyl)-1H-benzimidazole

1.2 Other means of identification

Product number -
Other names 1H-benzimidazole-2-carbaldehyde diethylacetal

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:13109-82-5 SDS

13109-82-5Relevant articles and documents

Photolysis of 4-Aryl-1H-oxadiazinobenzimidazoles

Rao, B. Ramamohan,Mohiuddin, G.,Ahmed, Khalil

, p. 158 - 159 (2007/10/02)

Photolysis of 4-aryl-1H-oxadiazinobenzimidazoles (I) in alcohols yields the corresponding benzimidazole-2-carboxaldehyde dialkyl acetals (III, R=CH3, C2H5) and aryl amides (IV) instead of the expected 1-oxo derivatives (II).A plausible mechanism involving the intermediacy of benzimidazole-2-carboxaldehyde (V) and aryl nitrile (VI) has been proposed.

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