4994-89-2 Usage
General Description
5,6-DIMETHYL-THIENO[2,3-D]PYRIMIDIN-4-YLAMINE is a chemical compound with a molecular formula C8H9N3S. It is a thieno pyrimidine derivative, which has a thienopyrimidine skeleton substituted with a dimethylamino group at position 4. 5,6-DIMETHYL-THIENO[2,3-D]PYRIMIDIN-4-YLAMINE is commonly used as a pharmaceutical intermediate in the synthesis of various drugs and pharmaceutical compounds. It exhibits biological activity and has potential applications in the development of new medications for various therapeutic indications. Its precise properties and uses depend on the specific application and formulations in which it is employed.
Check Digit Verification of cas no
The CAS Registry Mumber 4994-89-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,9 and 4 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4994-89:
(6*4)+(5*9)+(4*9)+(3*4)+(2*8)+(1*9)=142
142 % 10 = 2
So 4994-89-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H9N3S/c1-4-5(2)12-8-6(4)7(9)10-3-11-8/h3H,1-2H3,(H2,9,10,11)
4994-89-2Relevant articles and documents
Identification of 5,6-substituted 4-aminothieno[2,3-d]pyrimidines as LIMK1 inhibitors
Sleebs, Brad E.,Nikolakopoulos, George,Street, Ian P.,Falk, Hendrik,Baell, Jonathan B.
, p. 5992 - 5994 (2011/10/18)
4-Aminobenzothieno[3,2-d]pyrimidines were previously identified in a high throughput screening campaign as LIMK1 inhibitors. Scaffold reversal led to the identification of a series of simple 5,6-substituted 4-aminothieno[2,3-d] pyrimidines with low micromolar inhibition of LIMK1.
Synthesis and anti-microbial activity of some heterocycles: Part-II
Rahman, Khandker M. M.,Shaifullah Chowdhury,Bhuiyan,Hossain,Uddin
, p. 95 - 98 (2007/10/03)
Thieno[2,3-d]pyrimidines (2), (3) and (4) have been obtained via the reaction of 2-amino-4, 5-dimethylthiophen-3-carbonitrile (1) with formamide, acetonitrile and benzonitrile respectively. Treatment of (2), (3) and (4) with chloroacetaldehyde respectivel
