138189-51-2 Usage
Molecular weight
299.45 g/mol The relative molecular mass of the compound based on the atomic weights of its constituent elements.
Structure
Carbazole core with a substituted thiazolyl group The compound has a central carbazole ring system with a thiazolyl group attached to it, which contributes to its unique properties.
Heterocyclic compound
Yes The presence of multiple heteroatoms (nitrogen and sulfur) in the ring structure classifies 1H-Carbazole,
9-(4,5-dihydro-5,5-dimethyl-2-thiazolyl)-2,3,4,9-tetrahydro-6-methyl- as a heterocyclic compound.
Potential applications
Pharmaceutical industry and synthetic intermediate The compound has potential uses in drug development and as a building block for the synthesis of other complex molecules.
Research interest
New drug development and materials The presence of the thiazolyl group makes 1H-Carbazole,
9-(4,5-dihydro-5,5-dimethyl-2-thiazolyl)-2,3,4,9-tetrahydro-6-methyl- a promising candidate for further research in the development of new drugs and materials.
Unique structure and properties
Valuable target for chemical synthesis and scientific investigation The complex structure of the compound makes it an interesting target for synthesis and investigation in various fields of science and technology.
Check Digit Verification of cas no
The CAS Registry Mumber 138189-51-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,1,8 and 9 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 138189-51:
(8*1)+(7*3)+(6*8)+(5*1)+(4*8)+(3*9)+(2*5)+(1*1)=152
152 % 10 = 2
So 138189-51-2 is a valid CAS Registry Number.
138189-51-2Relevant academic research and scientific papers
Synthesis of 2-Amino-Substituted 4,5-Dihydro-1,3-thiazoles
Richter, C.,Hobert, A.,Meisner, W.,Schulze, K.
, p. 407 - 412 (2007/10/02)
The reaction of 2-substituted 4-methallylthiosemicarbazides 1 with carbonyl compounds catalyzed by weak acids gives the thiosemicarbazones 2 and 1,2,4-triazolidine-3-thiones 3.By contrats under strong acidic conditions the reaction occurs by electrophilic
