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138194-04-4

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138194-04-4 Usage

General Description

(5-Pyrid-4-ylthien-2-yl)methanol is a chemical compound with the molecular formula C11H9NOS. It consists of a pyridine ring and a thienyl group, both of which are attached to a central methanol molecule. (5-PYRID-4-YLTHIEN-2-YL)METHANOL has potential applications in the field of organic synthesis and pharmaceuticals, and its structure suggests that it may exhibit biological activity. The presence of both a pyridine and a thienyl group in its structure makes it a versatile building block for the synthesis of various organic compounds. Further research and exploration of its properties and potential uses could reveal new applications for this compound in the future.

Check Digit Verification of cas no

The CAS Registry Mumber 138194-04-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,1,9 and 4 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 138194-04:
(8*1)+(7*3)+(6*8)+(5*1)+(4*9)+(3*4)+(2*0)+(1*4)=134
134 % 10 = 4
So 138194-04-4 is a valid CAS Registry Number.

138194-04-4SDS

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 (5-pyridin-4-ylthiophen-2-yl)methanol

1.2 Other means of identification

Product number -
Other names -

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:138194-04-4 SDS

138194-04-4Downstream Products

138194-04-4Relevant articles and documents

Palladium-catalysed direct arylation of heteroaromatics bearing unprotected hydroxyalkyl functions using aryl bromides

Roger, Julien,Pozgan, Franc,Doucet, Henri

experimental part, p. 696 - 710 (2010/06/19)

Heteroaromatics bearing unprotected hydroxyalkyl functions can be arylated using aryl or heteroaryl bromides, via palladium-catalysed carbonhydrogen bond activation/arylation. Good yields were generally obtained using 0.01-0.5 mol% of the air-stable palladium acetate complex as the catalyst. The nature of the base was found to be crucial for the selectivity of this reaction. Potassium acetate led to the direct arylation products whereas caesium car-bonate led to the formation of the ether. This procedure is certainly more atom-economic than other methods for the preparation of such compounds, as no protection/ deprotection sequence of the hydroxyalkyl function and no preparation of an organometallic derivative is required.

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