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104617-86-9

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104617-86-9 Usage

Description

(±)-PraMipexole, also known as Pramipexole, is a recemic analogue of (S)-Pramipexole (P700755), which is a dopamine-D2-receptor agonist. It is a pharmaceutical compound that has been synthesized to target and activate specific dopamine receptors in the brain, playing a crucial role in the treatment of certain neurological conditions.

Uses

Used in Pharmaceutical Industry:
(±)-PraMipexole is used as an antiparkinsonian agent for the treatment of Parkinson's disease. It helps alleviate the symptoms of the disease by mimicking the effects of dopamine, a neurotransmitter that is often deficient in Parkinson's patients. This leads to improved motor function and a reduction in the severity of symptoms such as tremors, rigidity, and bradykinesia.
Additionally, (±)-PraMipexole has been found to have potential applications in other areas of medicine, such as the treatment of restless legs syndrome and certain types of depression. However, these uses are still under investigation and may require further research to confirm their efficacy and safety.

Check Digit Verification of cas no

The CAS Registry Mumber 104617-86-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,6,1 and 7 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 104617-86:
(8*1)+(7*0)+(6*4)+(5*6)+(4*1)+(3*7)+(2*8)+(1*6)=109
109 % 10 = 9
So 104617-86-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H17N3S/c1-2-5-12-7-3-4-8-9(6-7)14-10(11)13-8/h7,12H,2-6H2,1H3,(H2,11,13)

104617-86-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name S(-)-2-amino-6-propylamino-4,5,6,7-tetrahydrobenzothiazole

1.2 Other means of identification

Product number -
Other names (±)-pramipexole

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:104617-86-9 SDS

104617-86-9Relevant articles and documents

A preparation method of pramipexole hydrochloride (by machine translation)

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, (2019/02/04)

The invention discloses a method for preparation of pramipexole hydrochloride, comprises the following steps: to amino cyclohexyl [...] acyl chloride condensation for protecting amino group to obtain the propionyl cyclohexanol, then is obtained by catalyt

Bioisosteric heterocyclic versions of 7-{[2-(4-phenyl-piperazin-1-yl)ethyl] propylamino}-5,6,7,8-tetrahydronaphthalen-2-ol: Identification of highly potent and selective agonists for dopamine D3 receptor with potent in vivo activity

Biswas, Swati,Hazeldine, Stuart,Ghosh, Balaram,Parrington, Ingrid,Kuzhikandathil, Eldo,Reith, Maarten E. A.,Dutta, Aloke K.

experimental part, p. 3005 - 3019 (2009/04/06)

In the current report, we extend the SAR study on our hybrid structure 7-{[2-(4-phenyl-piperazin-1-yl)ethyl]propylamino}-5,6,7,8-tetrahydronaphthalen- 2-ol further to include heterocyclic bioisosteric analogues. Binding assays were carried out with HEK-29

METHOD FOR THE RESOLUTION OF 2-AMINO-6-PROPYLAMINO-4,5,6,7-TETRAHYDROBENZOTHIAZOL AND INTERMEDIATE COMPOUNDS

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Page/Page column 8, (2008/06/13)

The invention relates to a novel method for the resolution of the racemic mixture of compound (R,S)-2-amino-6-propylamino-4,5,6,7-tetrahydrobenzothiazole, or the enrichment of same with in one of its enantiomers, and to intermediate compounds which can be used to perform said method.

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