844891-11-8 Usage
Description
TERT-BUTYL 4-[4-(METHOXYCARBONYL)BENZYL]PIPERAZINE-1-CARBOXYLATE is a chemical compound with the molecular formula C23H32N2O4. It is a piperazine derivative featuring a tert-butyl group and a benzyl group with a methoxycarbonyl substituent. TERT-BUTYL 4-[4-(METHOXYCARBONYL)BENZYL]PIPERAZINE-1-CARBOXYLATE is primarily utilized in medicinal chemistry for the development of pharmaceutical agents, with a focus on central nervous system disorders. Additionally, it has been investigated for its potential as an anticancer agent and may possess other biological activities. Due to its potential biological activity and toxicity, special handling and precautions may be necessary.
Uses
Used in Pharmaceutical Development:
TERT-BUTYL 4-[4-(METHOXYCARBONYL)BENZYL]PIPERAZINE-1-CARBOXYLATE is used as a key intermediate in the synthesis of new pharmaceutical agents, particularly for the treatment of central nervous system disorders. Its unique structure allows for the development of drugs that can target specific neurological conditions.
Used in Anticancer Research:
In the field of oncology, TERT-BUTYL 4-[4-(METHOXYCARBONYL)BENZYL]PIPERAZINE-1-CARBOXYLATE is used as a potential anticancer agent. Its chemical properties are being studied to understand its effects on various types of cancer cells and to explore its potential as a therapeutic agent in cancer treatment.
Used in Medicinal Chemistry Research:
TERT-BUTYL 4-[4-(METHOXYCARBONYL)BENZYL]PIPERAZINE-1-CARBOXYLATE is also utilized in medicinal chemistry research to investigate its biological activities and to understand its mechanism of action. This knowledge can contribute to the design of more effective drugs and therapies for various diseases and conditions.
Used in Drug Delivery Systems:
TERT-BUTYL 4-[4-(METHOXYCARBONYL)BENZYL]PIPERAZINE-1-CARBOXYLATE may be employed in the development of drug delivery systems to improve the bioavailability and efficacy of pharmaceutical agents. Its chemical properties can be leveraged to enhance the delivery of drugs to target sites within the body, potentially improving treatment outcomes.
Used in Toxicology Studies:
Due to its potential biological activity and toxicity, TERT-BUTYL 4-[4-(METHOXYCARBONYL)BENZYL]PIPERAZINE-1-CARBOXYLATE is used in toxicology studies to assess its safety and side effects. This research is crucial for determining the appropriate dosages and administration methods for any pharmaceutical agents that incorporate this compound.
Used in Chemical Synthesis:
In the chemical industry, TERT-BUTYL 4-[4-(METHOXYCARBONYL)BENZYL]PIPERAZINE-1-CARBOXYLATE is used as a starting material or intermediate in the synthesis of various organic compounds. Its unique structure allows for the creation of a wide range of chemical products with diverse applications.
Check Digit Verification of cas no
The CAS Registry Mumber 844891-11-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,4,8,9 and 1 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 844891-11:
(8*8)+(7*4)+(6*4)+(5*8)+(4*9)+(3*1)+(2*1)+(1*1)=198
198 % 10 = 8
So 844891-11-8 is a valid CAS Registry Number.
InChI:InChI=1/C18H26N2O4/c1-18(2,3)24-17(22)20-11-9-19(10-12-20)13-14-5-7-15(8-6-14)16(21)23-4/h5-8H,9-13H2,1-4H3
844891-11-8Relevant articles and documents
LPAR1 Inhibitor. Medical application and preparation method thereof
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Paragraph 0072-0074; 0085-0086; 0091-0092, (2021/10/05)
LPAR1 Inhibitor, medical application and preparation method thereof, and the structural general formula I of the inhibitor is as follows. In-flight RX Alkyl groups selected from H, C1 - C6, COOCH3 , CF3 , NO2 ,
IRAK DEGRADERS AND USES THEREOF
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Paragraph 00962; 003516-003517, (2020/06/19)
The present invention provides compounds, compositions thereof, and methods of using the same.
Photoredox-catalyzed Direct Reductive Amination of Aldehydes without an External Hydrogen/Hydride Source
Alam, Rauful,Molander, Gary A.
supporting information, p. 2680 - 2684 (2018/05/22)
The direct reductive amination of aromatic aldehydes has been realized using a photocatalyst under visible light irradiation. The single electron oxidation of an in situ formed aminal species generates the putative α-amino radical that eventually delivers the reductive amination product. This method is operationally simple, highly selective, and functional group tolerant, which allows the direct synthesis of benzylic amines by a unique mechanistic pathway.
