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1H-BENZOIMIDAZOL-4-OL is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

67021-83-4

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67021-83-4 Usage

Chemical Properties

earthy yellow solid

Check Digit Verification of cas no

The CAS Registry Mumber 67021-83-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,0,2 and 1 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 67021-83:
(7*6)+(6*7)+(5*0)+(4*2)+(3*1)+(2*8)+(1*3)=114
114 % 10 = 4
So 67021-83-4 is a valid CAS Registry Number.
InChI:InChI=1/C7H6N2O/c10-6-3-1-2-5-7(6)9-4-8-5/h1-4,10H,(H,8,9)

67021-83-4SDS

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 1H-benzimidazol-4-ol

1.2 Other means of identification

Product number -
Other names 4-Hydroxy-1H-benzoimidazole

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:67021-83-4 SDS

67021-83-4Downstream Products

67021-83-4Relevant academic research and scientific papers

Microwave use of amidine compounds in the aqueous phase benzoate synthesis of benzimidazole compounds method

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Paragraph 0065, (2019/03/28)

The invention discloses a microwave the use of amidine compounds in the aqueous phase benzoate synthesis of benzimidazole compounds, in the aqueous phase under microwave conditions adding benzoic amidine compound under alkaline condition [...] into benzimidazole reaction, invention an environment-friendly, the operation is simple, cheap and safe, efficient process for preparing benzimidazole method. Compared with the prior art, this method not only can be applied to a large number of functional groups, the productive rate is high, few by-products, and the operation is simple, safe, low cost, environmental protection; .

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.

Substituted 4H-chromenes and analogs as activators of caspases and inducers of apoptosis and the use thereof

-

, (2008/06/13)

The present invention is directed to substituted 4H-chromenes and analogs thereof, represented by the general Formula I: 1wherein R1-R5, A, Y and Z are defined herein. The present invention also relates to the discovery that compounds having Formula I are activators of caspases and inducers of apoptosis. Therefore, the activators of caspases and inducers of apoptosis of this invention can be used to induce cell death in a variety of clinical conditions in which uncontrolled growth and spread of abnormal cells occurs.

Compositions for dyeing keratinous fiber

-

, (2008/06/13)

A composition for dyeing keratinous fiber which includes incorporated therein an oxidative color-developing substance, an enzyme which reacts with oxygen as a substrate but does not evolve hydrogen peroxide, and a weak reducing agent.

Synthesis of 4-Amino-7-hydroxybenzimidazole

Katritzky, Alan R.,Rachwal, Bogumila,Rachwal, Stanislaw,Steel, Peter J.,Zaklika, Krzysztof A.

, p. 2415 - 2422 (2007/10/02)

A simple and efficient synthesis of 4-amino-7-hydroxybenzimidazole (2a) was developed involving condensation of 2,3-diaminophenol with triethyl orthoformate, coupling the 4-hydroxybenzimidazole (6) thus obtained with 4-ethylbenzodiazonium chloride to give 4-(4-ethylphenylazo)-7-hydroxybenzimidazole (7) and hydrogenolysis of 7 to give 2a.Acetylation of 2a with acetic anhydride gave triacetyl derivative (8), the structure of which was proved by X-ray crystallographic analysis.

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