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856437-76-8

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856437-76-8 Usage

Chemical structure

BPP consists of a benzyl group attached to a piperazine ring and a propan-2-ol moiety.

Synonyms

BPP is also known as 1-BENZYLOXY-3-PIPERAZIN-1-YL-PROPAN-2-OL.

Pharmacological properties

BPP has been studied for its potential as a serotonin antagonist and dopamine agonist.

Potential applications

BPP has been investigated for its potential use in the treatment of certain neurological and psychiatric disorders.

Analgesic effects

BPP has shown potential for its analgesic (pain-relieving) properties.

Anti-inflammatory effects

BPP has demonstrated potential for its anti-inflammatory properties.

Preclinical studies

BPP has shown promise in preclinical studies, indicating its potential therapeutic benefits.

Further research

More research is needed to fully understand BPP's therapeutic potential and safety profile.

Molecular weight

The molecular weight of BPP is not provided in the material, but it can be calculated once the chemical formula is determined.

Check Digit Verification of cas no

The CAS Registry Mumber 856437-76-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,6,4,3 and 7 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 856437-76:
(8*8)+(7*5)+(6*6)+(5*4)+(4*3)+(3*7)+(2*7)+(1*6)=208
208 % 10 = 8
So 856437-76-8 is a valid CAS Registry Number.

856437-76-8Downstream Products

856437-76-8Relevant articles and documents

Microwave-assisted ring opening of epoxides: A general route to the synthesis of 1-aminopropan-2-ols with anti malaria parasite activities

Robin, Aélig,Brown, Fraser,Bahamontes-Rosa, Noemí,Wu, Binghua,Beitz, Eric,Kun, Jürgen F. J.,Flitsch, Sabine L.

, p. 4243 - 4249 (2008/02/12)

A series of 1-aminopropan-2-ols were synthesized and evaluated against two strains of malaria, Plasmodium falciparum FCR3 (chloroquine-resistant) and 3D7 (chloroquine-sensitive). Microwave-assisted ring opening of epoxides (aryl and alkyl glycidyl ethers,

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