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7-Methyltetrazolo[1,5-a]pyridine is a heterocyclic compound characterized by a tetrazolo[1,5-a]pyridine core structure, which features a pyridine ring fused to a tetrazole ring. The "7-methyl" part of its name indicates the presence of a methyl group (CH3) attached to the 7th position of the pyridine ring. 7-methyltetrazolo[1,5-a]pyridine is of interest in organic chemistry and medicinal chemistry due to its potential applications in the development of pharmaceuticals and other chemical products. It is known for its unique chemical properties and can be synthesized through various chemical reactions, making it a valuable building block in the creation of more complex molecules.

6635-33-2

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6635-33-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6635-33-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,3 and 5 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6635-33:
(6*6)+(5*6)+(4*3)+(3*5)+(2*3)+(1*3)=102
102 % 10 = 2
So 6635-33-2 is a valid CAS Registry Number.

6635-33-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-Methyl-tetradecansaeure-aethylester

1.2 Other means of identification

Product number -
Other names 6-Methyltetrazol<1,5-a>pyridin

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:6635-33-2 SDS

6635-33-2Relevant 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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