3034-57-9 Usage
Description
2-Amino-5-bromo-4-methylthiazole is an organic compound with the molecular formula C4H5BrN2S. It is a heterocyclic compound featuring a thiazole ring, which is a five-membered ring with one sulfur and one nitrogen atom. The presence of a bromine atom at the 5-position and a methyl group at the 4-position provides this compound with unique chemical and physical properties. It is a promising building block for the development of various materials and pharmaceuticals due to its versatile structure and reactivity.
Uses
Used in Solar Cell Applications:
2-Amino-5-bromo-4-methylthiazole is used as a synthetic building block for the development of poly(4-(p-alkoxystyryl)thiazole)s, which are polymers with potential applications in the field of solar energy. These polymers can be utilized as active layers in organic solar cells, where they play a crucial role in the conversion of sunlight into electrical energy. The incorporation of 2-Amino-5-bromo-4-methylthiazole into these polymers enhances their light absorption properties and improves the overall efficiency of the solar cells.
Check Digit Verification of cas no
The CAS Registry Mumber 3034-57-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,3 and 4 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3034-57:
(6*3)+(5*0)+(4*3)+(3*4)+(2*5)+(1*7)=59
59 % 10 = 9
So 3034-57-9 is a valid CAS Registry Number.
InChI:InChI=1/C4H5BrN2S/c1-2-3(5)8-4(6)7-2/h1H3,(H2,6,7)
3034-57-9Relevant articles and documents
Synthesis, biological evaluation and molecular modeling study of some new thiazolodiazepine analogs as CNS active agents
Al-Rashood, Sarah T.A.,Hassan, Ghada S.,El-Messery, Shahenda M.,El-Taher, Kamal E.H.,Hefnawy, Mohamed M.,Al-Omar, Mahmmed A.,El-Subbagh, Hussein I.
supporting information, p. 445 - 453 (2016/01/09)
New derivatives of ethyl 8-oxo-5,6,7,8-tetrahydro-thiazolo[3,2-a][1,3]diazepin-3-carboxylate (HIE-124, 3), were synthesized as continuation to our previous patented efforts. Compounds 15 and 20 showed marginal hypnotic potency compared to 3. Compounds 15 (0.78 mmol/kg) and 20 (0.39 mmol/kg) showed remarkable 100% protection against PTZ induced convulsions with two and four fold increase in activity than sodium valproate (1.38 mmol/kg), respectively. Molecular modeling studies showed hydrogen bonding interaction between 15 and Thr56 residues at the binding site of GABAA. Superposition, flexible alignment and surface mapping of 15, 20 and diazepam supports their biological resemblance where ADMET study suggested that those compounds could be used as oral anticonvulsants.
4-methylthiazole derivatives, their methods of preparation and the pharmaceutical compositions in which they are present
-
, (2008/06/13)
The present invention relates to novel 4-methylthiazole derivatives, to tr methods of preparation and to the pharmaceutical compositions in which they are present. According to the invention, these derivatives have the general formula STR1 in which n is e