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58885-00-0

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58885-00-0 Usage

Class of compound

Heterocyclic

Containing elements

Nitrogen, Fluorine

Potential applications

Pharmaceuticals, Agrochemicals

Use as building block

Synthesis of biologically active molecules

Trifluoromethyl group significance

Valuable reagent for introducing fluorine atoms

Importance in research

Interesting target for organic chemistry development

Check Digit Verification of cas no

The CAS Registry Mumber 58885-00-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,8,8 and 5 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 58885-00:
(7*5)+(6*8)+(5*8)+(4*8)+(3*5)+(2*0)+(1*0)=170
170 % 10 = 0
So 58885-00-0 is a valid CAS Registry Number.

58885-00-0SDS

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-(trifluoromethyl)-1H-imidazo[4,5-b]pyrazine

1.2 Other means of identification

Product number -
Other names 2-(trifluoromethyl)-1H-imidazo[4.5-b]pyrazine

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:58885-00-0 SDS

58885-00-0Downstream Products

58885-00-0Relevant articles and documents

Efficient syntheses of 2-fluoroalkylbenzimidazoles and -benzothiazoles

René, Olivier,Souverneva, Alexandra,Magnuson, Steven R.,Fauber, Benjamin P.

supporting information, p. 201 - 204 (2013/02/22)

We report an efficient one-step route to 2-fluoroalkylbenzimidazoles and -benzothiazoles via the condensation of fluorinated carboxylic acids and aromatic diamines or aminothiophenols. Additionally, we describe the syntheses of fluoroalkyl-azabenzimidazoles, -purines, and -imidazolopyrazines. This method is high-yielding with broad scope and is operationally simple with potential application to parallel synthesis.

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