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5,5-dimethyl-3-(6-phenylhex-3-yn-1-yl)-1,3-thiazolidine-2,4-dione is a complex organic compound characterized by a unique molecular structure. It features a 1,3-thiazolidine-2,4-dione core, which is a heterocyclic ring system containing sulfur and oxygen atoms. The molecule is further distinguished by two methyl groups attached to the 5-position of the thiazolidine ring, contributing to its steric properties. A 6-phenylhex-3-yn-1-yl group is attached to the 3-position, which includes a phenyl ring and a hex-3-yn-1-yl chain, the latter being a hexyl group with a triple bond at the third carbon. This structural arrangement endows the compound with specific chemical and physical properties, making it a potential candidate for various applications in fields such as pharmaceuticals, materials science, or as a chemical intermediate.

86106-16-3

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86106-16-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86106-16-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,1,0 and 6 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 86106-16:
(7*8)+(6*6)+(5*1)+(4*0)+(3*6)+(2*1)+(1*6)=123
123 % 10 = 3
So 86106-16-3 is a valid CAS Registry Number.

86106-16-3Relevant academic research and scientific papers

THIA-ACYLIMINIUM - OLEFIN CYCLIZATIONS

Hamersma, J. A. M.,Speckamp, W. N.

, p. 3255 - 3266 (2007/10/02)

Regioselective NaBH4/H(1+)-reduction of thiazolidine-diones 3 - 8 substituted at the nitrogen atom with different ?-nucleophiles affords hydroxylactams 9 - 14 in good yields.The latter compounds are excellent precursors for the α-acyliminium ion 16 and ca

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