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5-methyltetrazolo[1,5-a]pyridine is a heterocyclic compound characterized by a tetrazolo[1,5-a]pyridine ring system with a methyl group attached at the 5th position. This nitrogen-rich molecule is known for its potential applications in medicinal chemistry, particularly as a building block for the synthesis of various biologically active compounds. The structure of 5-methyltetrazolo[1,5-a]pyridine features a central pyridine ring fused to a tetrazolo ring, which contributes to its stability and reactivity. Its chemical properties make it a valuable intermediate in the development of new drugs and pharmaceuticals, as it can be further functionalized to create a range of derivatives with diverse therapeutic properties.

6624-45-9

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6624-45-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6624-45-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,2 and 4 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6624-45:
(6*6)+(5*6)+(4*2)+(3*4)+(2*4)+(1*5)=99
99 % 10 = 9
So 6624-45-9 is a valid CAS Registry Number.
InChI:InChI=1/C6H6N4/c1-5-3-2-4-6-7-8-9-10(5)6/h2-4H,1H3

6624-45-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-methyltetrazolo[1,5-a]pyridine

1.2 Other means of identification

Product number -
Other names 5-methyl-tetrazolopyridin

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

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More Details:6624-45-9 SDS

6624-45-9Relevant academic research and scientific papers

Reaction of N-fluoropyridinium fluoride with isonitriles and TMSN 3: A convenient one-pot synthesis of tetrazol-5-yl pyridines

Kiselyov, Alexander S.

, p. 4851 - 4854 (2007/10/03)

Reaction of N-fluoropyridinium fluoride generated in situ with a series of isonitriles and TMSN3 led to the formation of the corresponding tetrazol-5-yl pyridines in good yields (37-84%). A similar reaction sequence for quinoline yielded the respective derivatives of 2-quinoline. The proposed reaction mechanism involves the intermediate formation of a highly reactive carbene species.

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