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1393886-88-8

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1393886-88-8 Usage

General Description

(S)-N6-[2-(trans-4-AMinocyclohexyl)ethyl]-N6-propyl-4,5,6,7-tetrahydrobenzothiazole-2,6-diaMine is a chemical compound with a complex molecular structure. It contains a cyclohexyl group, a propyl group, and a tetrahydrobenzothiazole ring. (S)-N6-[2-(trans-4-AMinocyclohexyl)ethyl]-N6-propyl-4,5,6,7-tetrahydrobenzothiazole-2,6-diaMine also contains two amine groups, one at the 2-position and the other at the 6-position of the benzothiazole ring. The trans-4-aminocyclohexyl group is also attached to the benzothiazole ring. This chemical may have potential applications in pharmaceuticals, agrochemicals, or as a reagent for chemical synthesis. It is important to handle and use this compound with caution, as it may present hazardous properties and should be used in accordance with safety guidelines and regulations.

Check Digit Verification of cas no

The CAS Registry Mumber 1393886-88-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,9,3,8,8 and 6 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1393886-88:
(9*1)+(8*3)+(7*9)+(6*3)+(5*8)+(4*8)+(3*6)+(2*8)+(1*8)=228
228 % 10 = 8
So 1393886-88-8 is a valid CAS Registry Number.

1393886-88-8Upstream product

1393886-88-8Downstream Products

1393886-88-8Relevant articles and documents

Design, synthesis, and evaluation of potent and selective ligands for the dopamine 3 (D3) receptor with a novel in vivo behavioral profile

Chen, Jianyong,Collins, Gregory T.,Zhang, Jian,Yang, Chao-Yie,Levant, Beth,Woods, James,Wang, Shaomeng

supporting information; experimental part, p. 5905 - 5908 (2009/09/29)

A series of compounds structurally related to pramipexole were designed, synthesized, and evaluated as ligands for the dopamine 3 (D3) receptor. Compound 12 has a Ki value of 0.41 nM to D3 and a selectivity of > 30000- and 800-fold over the D1-like and D 2 receptors, respectively. Our in vivo functional assays showed that this compound is a partial agonist at the D3 receptor with no detectable activity at the D2 receptor.

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