162045-48-9 Usage
Description
1-BOC-4-[(2-HYDROXYPHENYL)AMINO]-PIPERIDINE is a synthetic compound characterized by a piperidine ring with a 2-hydroxyphenylamino group at the 4-position and a BOC protecting group on the nitrogen atom. This structure endows the compound with potential biological activity and utility in various applications, particularly in the pharmaceutical and materials chemistry fields.
Uses
Used in Pharmaceutical Industry:
1-BOC-4-[(2-HYDROXYPHENYL)AMINO]-PIPERIDINE is used as a building block for the synthesis of new drug candidates due to its unique structure and the presence of the 2-hydroxyphenylamino group, which may contribute to biological activity.
Used in Medicinal Chemistry:
1-BOC-4-[(2-HYDROXYPHENYL)AMINO]-PIPERIDINE is used as a precursor in the development of pharmaceutical compounds, leveraging its potential antioxidant and anti-inflammatory properties stemming from the phenolic group.
Used in Materials Chemistry:
1-BOC-4-[(2-HYDROXYPHENYL)AMINO]-PIPERIDINE is used as a component in the creation of larger molecules or materials, taking advantage of its structural features to enhance the properties of the final product.
Further investigation into the properties and potential applications of 1-BOC-4-[(2-HYDROXYPHENYL)AMINO]-PIPERIDINE is necessary to fully explore its capabilities and maximize its utility in these fields.
Check Digit Verification of cas no
The CAS Registry Mumber 162045-48-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,2,0,4 and 5 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 162045-48:
(8*1)+(7*6)+(6*2)+(5*0)+(4*4)+(3*5)+(2*4)+(1*8)=109
109 % 10 = 9
So 162045-48-9 is a valid CAS Registry Number.
InChI:InChI=1/C16H24N2O3/c1-16(2,3)21-15(20)18-10-8-12(9-11-18)17-13-6-4-5-7-14(13)19/h4-7,12,17,19H,8-11H2,1-3H3
162045-48-9Relevant articles and documents
DIPHENYLBUTYPIPERIDINE AUTOPHAGY INDUCERS
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Page/Page column 7; 87-90, (2011/12/02)
Autophagy inducing compounds, methods of their preparation and use, and kits containg said compounds are disclosed herein.
Piperidine amides as 11β-hydroxysteroid dehydrogenase type 1 inhibitors
Flyrén, Katarina,Bergquist, Lars O.,Castro, Victor M.,Fotsch, Christopher,Johansson, Lars,St. Jean Jr., David J.,Sutin, Lori,Williams, Meredith
, p. 3421 - 3425 (2008/02/08)
A series of piperidine amide inhibitors of human 11β-hydroxysteroid dehydrogenase type 1 (11β-HSD1) were identified via modifications of the HTS hit compound 1. The synthesis, in vitro biological evaluation, and structure-activity relationship of these co
Phenoxyalkylamine derivatives useful as opioid receptor agonists
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, (2008/06/13)
A medicament useful for preventive and/or therapeutic treatment of nerve system diseases which comprises, as an active ingredient, a compound represented by the following general formula (I) or a pharmacologically acceptable salt thereof: wherein, X represents a group represented by the following general formula (II), (III), (IV), (V), or (VI), “A” represents a saturated or unsaturated 3- to 6-membered carbocyclic group and the like, “B” represents CH2 and the like, “n” represents 0 to 2, R1 represents a hydrogen atom, a halogen atom and the like, R2, R3, and R7 to R14 represent a hydrogen atom, a lower alkyl group which may be substituted and the like, R4 represents a hydrogen atom, a lower alkyl group which may be substituted and the like, R5 represents a hydrogen atom, a halogen atom and the like, R6 represents a saturated or unsaturated monocyclic or bicyclic carbocyclic group and the like, and R5 and R6, R7 and R8, R9 and R10, or R11 and R12 may bind to each other to form a cyclic structure.
