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5340-04-5

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5340-04-5 Usage

General Description

1-PROPYL-1H-TETRAZOL-5-YLAMINE is a chemical compound with the molecular formula C6H12N4. It is a propyl derivative of tetrazole, containing a propyl group attached to the nitrogen atom in the tetrazole ring. 1-PROPYL-1H-TETRAZOL-5-YLAMINE is used in organic synthesis, pharmaceutical research, and as a building block for the preparation of various biologically active compounds. It is also used as a reagent in chemical reactions and as a precursor for the synthesis of heterocyclic compounds. As a propyl derivative of tetrazole, it exhibits similar properties and reactivity to other tetrazole compounds, making it valuable in various chemical and pharmaceutical applications.

Check Digit Verification of cas no

The CAS Registry Mumber 5340-04-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,4 and 0 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5340-04:
(6*5)+(5*3)+(4*4)+(3*0)+(2*0)+(1*4)=65
65 % 10 = 5
So 5340-04-5 is a valid CAS Registry Number.
InChI:InChI=1/C4H9N5/c1-2-3-9-4(5)6-7-8-9/h2-3H2,1H3,(H2,5,6,8)

5340-04-5 Well-known Company Product Price

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  • Aldrich

  • (CBR00443)  1-Propyl-1H-tetrazol-5-amine  AldrichCPR

  • 5340-04-5

  • CBR00443-1G

  • 2,255.76CNY

  • Detail

5340-04-5Relevant articles and documents

9H-Xanthene-9-carboxylic acid [1,2,4]oxadiazol-3-yl- and (2H-tetrazol-5-yl)-amides as potent, orally available mGlu1 receptor enhancers

Vieira, Eric,Huwyler, Joerg,Jolidon, Synese,Knoflach, Frederic,Mutel, Vincent,Wichmann, Juergen

, p. 4628 - 4631 (2007/10/03)

Small molecule mGluR1 enhancers based on the lead compound (9H-xanthene-9-carbonyl)-carbamic acid butyl ester derived from random-screening hit diphenylacetyl-carbamic acid ethyl ester were designed and synthesized as useful pharmacological tools for the study of the physiological roles mediated by mGlu1 receptors. The synthesis and the structure-activity relationship of this new class of positive allosteric modulators of mGlu1 receptors will be discussed in detail.

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