31602-63-8 Usage
General Description
C-(2H-tetrazol-5-yl)-methylamine, also known as C-Tetra, is a chemical compound with the molecular formula C3H7N5. It is a white crystalline powder that is commonly used as a building block in organic synthesis and pharmaceutical research. C-Tetra has been studied for its potential as a central nervous system stimulant and has also been investigated for its antibiotic and antiparasitic properties. C-(2H-TETRAZOL-5-YL)-METHYLAMINE is known for its stability and relatively low toxicity, making it a valuable tool for drug discovery and medicinal chemistry. However, it should be handled and stored with care, as it can be hazardous if not used properly.
Check Digit Verification of cas no
The CAS Registry Mumber 31602-63-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,6,0 and 2 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 31602-63:
(7*3)+(6*1)+(5*6)+(4*0)+(3*2)+(2*6)+(1*3)=78
78 % 10 = 8
So 31602-63-8 is a valid CAS Registry Number.
InChI:InChI=1/C2H5N5/c3-1-2-4-6-7-5-2/h1,3H2,(H,4,5,6,7)
31602-63-8Relevant articles and documents
Synthesis and preliminary evaluation of amiloride analogs as inhibitors of the urokinase-type plasminogen activator (uPA)
Matthews, Hayden,Ranson, Marie,Tyndall, Joel D.A.,Kelso, Michael J.
scheme or table, p. 6760 - 6766 (2011/12/05)
A known side-activity of the oral potassium-sparing diuretic drug amiloride is inhibition of the enzyme urokinase-type plasminogen activator (uPA, K i = 7 μM), a promising anticancer target. Several studies have demonstrated significant antitum
Synthesis of tetrazole analogues of amino acids using Fmoc chemistry: isolation of amino free tetrazoles and their incorporation into peptides
Sureshbabu, Vommina V.,Venkataramanarao, Rao,Naik, Shankar A.,Chennakrishnareddy
, p. 7038 - 7041 (2008/03/12)
An efficient synthesis of tetrazole analogues of amino acids starting from Nα-Fmoc amino acid in a three-step protocol is reported. The free amino tetrazoles were obtained in good yields and with excellent purity after removal of the Fmoc group