Product Name:1-cyclopropylpiperazine

IUPAC Name:1-cyclopropylpiperazine

CAS:20327-23-5
Molecular Formula:C7H14N2
Purity:95%+
Catalog Number:CM102401
Molecular Weight:126.2

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CM102401-10g in stock ǑŪ
CM102401-25g in stock ȅǑƃ
CM102401-100g in stock Şȅƴ

For R&D use only.

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Product Details

CAS NO:20327-23-5
Molecular Formula:C7H14N2
Melting Point:-
Smiles Code:N1(C2CC2)CCNCC1
Density:
Catalog Number:CM102401
Molecular Weight:126.2
Boiling Point:200°C at 760 mmHg
MDL No:MFCD06254805
Storage:Store at 2-8°C.

Category Infos

Piperazines
Piperazine is an organic compound consisting of a six-membered ring containing two nitrogen atoms in opposite positions in the ring. The chemical formula of piperazine is C4H10N2, and it is an important pharmaceutical intermediate. Pyrimidines and piperazines are known to be the backbone of many bulk compounds and important core structures for approved drugs; studies have shown that combining a pyridine ring with a piperazine moiety within a single structural framework enhances biological activity.
Cyclopropanes
Cyclopropane is the smallest cyclic compound with unique structural features and physicochemical properties, which is widely used in the design of small molecule drugs. In drug design, it is often used to increase activity, fix conformation and improve PK and water solubility. The introduction of cyclopropyl groups into drugs can change various properties of molecules, such as improving metabolic stability; increasing biological activity; enhancing drug efficacy; limiting polypeptide conformation and slowing down its hydrolysis; reducing plasma clearance; improving drug dissociation and many more. Cyclopropane rings are widely found in marketed drugs, including cardiovascular drugs, central nervous system (CNS) drugs, anticancer drugs, autoimmune and anti-inflammatory drugs.

Column Infos

RMC-9805
Revolution Medicines announced preliminary positive data for its RAS(ON) G12D-selective covalent inhibitor RMC-9805 in previously treated pancreatic ductal adenocarcinoma (PDAC) patients. The analysis showed that the disease control rate of PDAC patients treated with RMC-9805 was as high as 80%. RMC-9805 is a potential ‘first-in-class’ oral RAS(ON) G12D-selective inhibitor, that is being evaluated in trials to examine its efficacy and safety in patients with solid tumors carrying KRAS G12D mutations when used as a single agent or in combination with the pan-RAS inhibitor RMC-6236.
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