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Structure of 950194-37-3
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This chiral heterocycle features a rigid, electron-deficient scaffold that integrates seamlessly into asymmetric synthesis. The (S)-configuration at the benzylic center imparts distinct stereochemical control in catalytic transformations, while the fused imidazothiazole core enhances metabolic stability and binding affinity for target proteins.
(S)-2-Phenyl-2,3-dihydrobenzo[d]imidazo[2,1-b]thiazole serves as a rigid, chiral heterocyclic scaffold with defined stereochemistry at the 2-position. It functions as a versatile building block in medicinal chemistry, enabling access to bioactive molecules through functionalization at the phenyl and thiazole moieties. The compound exhibits bench stability and compatibility with standard coupling reactions, facilitating downstream derivatization in target-oriented synthesis.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H315-H319-H335
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Precautionary Statements : P233-P260-P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P340-P362-P403-P405-P501
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Lot numbers can be found on the outside label of a product: