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3-methyl-1-(piperidin-1-yl)butane-1-thione is an organic compound with the molecular formula C11H21NS. It is a colorless liquid with a strong, pungent odor. 3-methyl-1-(piperidin-1-yl)butane-1-thione is characterized by the presence of a thioether functional group, which consists of a sulfur atom bonded to two alkyl groups. The molecule features a 3-methylbutane chain with a piperidine ring attached to the first carbon atom. The piperidine ring is a six-membered nitrogen-containing ring, which contributes to the compound's unique chemical properties. 3-methyl-1-(piperidin-1-yl)butane-1-thione is used in the synthesis of various pharmaceuticals and agrochemicals due to its versatile chemical structure and reactivity.

5310-01-0

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5310-01-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5310-01-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,1 and 0 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5310-01:
(6*5)+(5*3)+(4*1)+(3*0)+(2*0)+(1*1)=50
50 % 10 = 0
So 5310-01-0 is a valid CAS Registry Number.

5310-01-0Downstream Products

5310-01-0Relevant articles and documents

Aqueous Compatible Protocol to Both Alkyl and Aryl Thioamide Synthesis

Wei, Jianpeng,Li, Yiming,Jiang, Xuefeng

, p. 340 - 343 (2016)

An efficient aqueous synthesis of thioamides through aldehydes, sodium sulfide, and N-substituted formamides has been developed. Both alkyl and aryl aldehydes are amenable to this protocol. N-Substituted formamides are essential for this transformation. Readily available inorganic salt (sodium sulfide) serves as the sulfur source in water, which makes this method much more practical and efficient. Furthermore, the late-stage modification of bioactive molecules and derivatives through this protocol has been established.

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