844891-11-8 Usage
General Description
TERT-BUTYL 4-[4-(METHOXYCARBONYL)BENZYL]PIPERAZINE-1-CARBOXYLATE is a chemical compound with the molecular formula C23H32N2O4. It is a piperazine derivative with a tert-butyl group, and a benzyl group with a methoxycarbonyl substituent. TERT-BUTYL 4-[4-(METHOXYCARBONYL)BENZYL]PIPERAZINE-1-CARBOXYLATE is commonly used in medicinal chemistry for the development of new pharmaceutical agents, particularly in the area of central nervous system disorders. It has also been studied for its potential as an anticancer agent, and it may have other biological activities as well. This chemical may require special handling and precautions due to its potential biological activity and toxicity.
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
-
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
-
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.
