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5,5,8,8-Tetramethyl-5,6,7,8-tetrahydronaphthalen-2-ylamine, also known as 5,5,8,8-Tetramethyl-5,6,7,8-tetrahydronaphthalen-2-amine, is a chemical compound belonging to the amine family with the molecular formula C16H25N. It is an amine derivative characterized by a unique molecular structure featuring a tetramethyl substitution on the aromatic ring and a tetrahydronaphthalen-2-ylamine moiety. 5,5,8,8-Tetramethyl-5,6,7,8-tetrahydronaphthalen-2-ylamine has potential applications in pharmaceuticals and medicinal chemistry due to its structural features and may exhibit biological activity that warrants further research and development.

92050-16-3

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92050-16-3 Usage

Uses

Used in Pharmaceutical Industry:
5,5,8,8-Tetramethyl-5,6,7,8-tetrahydronaphthalen-2-ylamine is used as a chemical intermediate for the synthesis of various pharmaceutical compounds. Its unique molecular structure allows for the development of new drugs with potential therapeutic applications.
Used in Medicinal Chemistry Research:
5,5,8,8-Tetramethyl-5,6,7,8-tetrahydronaphthalen-2-ylamine serves as a valuable compound in medicinal chemistry research. Its structural features can be utilized to design and develop novel molecules with potential biological activities, contributing to the discovery of new therapeutic agents.
Used in Drug Synthesis:
As a chemical compound with a tetramethyl substitution and a tetrahydronaphthalen-2-ylamine moiety, 5,5,8,8-Tetramethyl-5,6,7,8-tetrahydronaphthalen-2-ylamine can be employed in the synthesis of various drugs. Its unique structure may contribute to the development of new pharmaceuticals with improved efficacy and safety profiles.
Used in Drug Design:
5,5,8,8-Tetramethyl-5,6,7,8-tetrahydronaphthalen-2-ylamine can be utilized in drug design to create molecules with specific biological activities. Its structural features can be modified to optimize the pharmacological properties of the resulting compounds, leading to the development of innovative therapeutic agents.
Used in Chemical Synthesis:
5,5,8,8-Tetramethyl-5,6,7,8-tetrahydronaphthalen-2-ylamine can be employed as a starting material or intermediate in various chemical synthesis processes. Its unique molecular structure allows for the production of a wide range of chemical compounds with diverse applications in different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 92050-16-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,0,5 and 0 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 92050-16:
(7*9)+(6*2)+(5*0)+(4*5)+(3*0)+(2*1)+(1*6)=103
103 % 10 = 3
So 92050-16-3 is a valid CAS Registry Number.
InChI:InChI=1/C14H21N/c1-13(2)7-8-14(3,4)12-9-10(15)5-6-11(12)13/h5-6,9H,7-8,15H2,1-4H3

92050-16-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 5,5,8,8-tetramethyl-6,7-dihydronaphthalen-2-amine

1.2 Other means of identification

Product number -
Other names 1,1,4,4-tetramethyl-1,2,3,4-tetrahydro-naphth-6-ylamine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:92050-16-3 SDS

92050-16-3Downstream Products

92050-16-3Relevant academic research and scientific papers

Synthesis of Tamibarotene via Ullmann-Type Coupling

Bao, Xuefei,Qiao, Xuejun,Bao, Changshun,Liu, Yuting,Zhao, Xuan,Lu, Yi,Chen, Guoliang

, p. 748 - 753 (2017)

An effective process was developed for the preparation of tamibarotene via an Ullmann-type coupling in a nonpressurized l-proline/DMSO system. Notable features were the telescoping of reactions, avoiding environmentally hazardous materials, and an accepta

C-H Amination of Arenes with Hydroxylamine

See, Yi Yang,Sanford, Melanie S.

supporting information, p. 2931 - 2934 (2020/04/09)

This Letter describes the development of a TiIII-mediated reaction for the C-H amination of arenes with hydroxylamine. This reaction is applied to a variety of electron-rich (hetero)arene substrates, including a series of natural products and pharmaceuticals. It offers the advantages of mild conditions (room temperature), fast reaction rates (30 min), compatibility with ambient moisture and air, scalability, and the use of inexpensive commercial reagents.

The cubane paradigm in bioactive molecule discovery: Further scope, limitations and the cyclooctatetraene complement

Houston, Sevan D.,Fahrenhorst-Jones, Tyler,Xing, Hui,Chalmers, Benjamin A.,Sykes, Melissa L.,Stok, Jeanette E.,Farfan Soto, Clementina,Burns, Jed M.,Bernhardt, Paul V.,De Voss, James J.,Boyle, Glen M.,Smith, Maree T.,Tsanaktsidis, John,Savage, G. Paul,Avery, Vicky M.,Williams, Craig M.

, p. 6790 - 6798 (2019/07/22)

The cubane phenyl ring bioisostere paradigm was further explored in an extensive study covering a wide range of pharmaceutical and agrochemical templates, which included antibiotics (cefaclor, penicillin G) and antihistamine (diphenhydramine), a smooth muscle relaxant (alverine), an anaesthetic (ketamine), an agrochemical instecticide (triflumuron), an antiparasitic (benznidazole) and an anticancer agent (tamibarotene). This investigation highlights the scope and limitations of incorporating cubane into bioactive molecule discovery, both in terms of synthetic compatibility and physical property matching. Cubane maintained bioisosterism in the case of the Chagas disease antiparasitic benznidazole, although it was less active in the case of the anticancer agent (tamibarotenne). Application of the cyclooctatetraene (COT) (bio)motif complement was found to optimize benznidazole relative to the benzene parent, and augmented anticancer activity relative to the cubane analogue in the case of tamibarotene. Like all bioisosteres, scaffolds and biomotifs, however, there are limitations (e.g. synthetic implementation), and these have been specifically highlighted herein using failed examples. A summary of all templates prepared to date by our group that were biologically evaluated strongly supports the concept that cubane is a valuable tool in bioactive molecule discovery and COT is a viable complement.

Copper(ii)-catalyzed c-n coupling of aryl halides and n-nucleophiles promoted by quebrachitol or diethylene glycol

Chen, Guoliang,Chen, Yuanguang,Du, Fangyu,Fu, Yang,Wu, Ying,Zhou, Qifan

supporting information, p. 2161 - 2168 (2019/11/25)

Herein, we report the natural ligand quebrachitol (QCT) as a promoter for a Cu(II) catalyst, which is highly effective for N-Arylation of various amines and related aryl halides. A series of diarylamine derivatives were obtained in high yields by using diethylene glycol (DEG) as both ligand and solvent. The C-N coupling reactions proceed under mild conditions and exhibit good functional group tolerance.

DIHYDROINDENE AND TETRAHYDRONAPHTHALENE COMPOUNDS

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Paragraph 0114; 0119, (2018/08/09)

The invention provides compounds of formula I: and salts thereof, as well as pharmaceutical compositions comprising such compounds. The compounds are useful for treating cancers, Alzheimer's disease, and conditions associated with demyelination.

Design, synthesis and anticancer biological evaluation of novel 1,4-diaryl-1,2,3-triazole retinoid analogues of tamibarotene (AM80)

Aleixo, Mariana A. A.,Garcia, Taís M.,Carvalho, Diego B.,Viana, Luiz H.,Amaral, Marcos S.,Kassab, Najla M.,Cunha, Marilin C.,Pereira, Indiara C.,Guerrero, Palimécio G,Perdomo, Renata T.,Matos, Maria F. C.,Baroni, Adriano C. M.

, p. 109 - 124 (2017/12/08)

We report herein the design and synthesis via click chemistry of twelve novel triazole retinoid analogues of tamibarotene (AM80) and the evaluation of their anticancer activities against six cancer cell lines: HL60, K562, 786, HT29, MCF7 and PC3. Among the synthesized compounds, two were more potent than tamibarotene against solid tumor cells, and one of them had similar potency to tamibarotene against HL60 cells. The bioisosteric exchange between the amide group and the 1,2,3-triazole core in the retinoid agent tamibarotene (AM80) reported in this work is a valid strategy for the generation of useful compounds against cancer.

ANTICANCER AGENT DELIVERY MOLECULE

-

, (2017/08/04)

PROBLEM TO BE SOLVED: To provide a compound which can be used as an anticancer agent targeting a cancer cell that highly expresses Lysine-specific demethylase 1 (LSD1) or salt thereof. SOLUTION: The present invention provides a compound represented by the following formula (I) or a pharmaceutically acceptable salt thereof, where Ar, R1, R2, L, Z, p, q, *1 and *2 are as defined in the specifications. SELECTED DRAWING: None COPYRIGHT: (C)2017,JPOandINPIT

Modeling, Synthesis, and Biological Evaluation of Potential Retinoid X Receptor (RXR)-Selective Agonists: Analogues of 4-[1-(3,5,5,8,8-Pentamethyl-5,6,7,8-tetrahydro-2-naphthyl)ethynyl]benzoic Acid (Bexarotene) and 6-(Ethyl(5,5,8,8-tetrahydronaphthalen-2-yl)amino)nicotinic Acid (NEt-TMN)

Heck, Michael C.,Wagner, Carl E.,Shahani, Pritika H.,Macneill, Mairi,Grozic, Aleksandra,Darwaiz, Tamana,Shimabuku, Micah,Deans, David G.,Robinson, Nathan M.,Salama, Samer H.,Ziller, Joseph W.,Ma, Ning,Van Der Vaart, Arjan,Marshall, Pamela A.,Jurutka, Peter W.

supporting information, p. 8924 - 8940 (2016/10/22)

Sulfonic acid analogues of 4-[1-(3,5,5,8,8-pentamethyl-5,6,7,8-tetrahydro-2-naphthyl)ethynyl]benzoic acid (bexarotene, 1) as well as seven novel and two reported analogues of 6-(ethyl(5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphthalen-2-yl)amino)nicotinic acid (NEt-TMN) were synthesized and assessed for selective retinoid X receptor (RXR) agonism. Compound 1 is FDA-approved for treatment of cutaneous T-cell lymphoma (CTCL); however, 1 can provoke side effects by impacting RXR-dependent receptor pathways. All of the analogues in this study were evaluated for their potential to bind RXR through modeling and then assayed in an RXR-RXR mammalian-2-hybrid (M2H) system and in RXR-responsive element (RXRE)-mediated transcriptional experiments. The EC50 profiles for these unique analogues and their analogous effectiveness to inhibit proliferation in CTCL cells relative to 1 suggest that these compounds possess similar or even enhanced therapeutic potential. Several compounds also displayed more selective RXR activation with minimal cross-signaling of the retinoic acid receptor. These results suggest that modifications of potent RXR agonists such as NEt-TMN can lead to improved biological selectivity and potency compared with the known therapeutic.

Design, synthesis and biological evaluation of novel tamibarotene derivative as multitarget anticancer agent

Jiang, Yuqi,Hou, Jinning,Li, Xiaoyang,Xu, Wenfang,Zhang, Yingjie

, p. 729 - 733 (2016/09/28)

A novel tamibarotene derivative was synthesized by coupling cytotoxic agent 5-Fluorouracil (5-FU) with tamibarotene via ester. This hybrid drug (compound 10) was evaluated for its antiproliferative activities against human leukemic U937, HL-60 and K562 cell lines in vitro. Results showed that compound 10 exhibited more potent anti-leukemic activity than the positive control tamibarotene. Furthermore, the preliminary stability test of compound 10 revealed that it could release tamibarotene and 5-FU significantly in vitro. These interesting results would be meaningful to develop more potent drugs for the treatment of human leukemia.

THERAPEUTIC COMPOUNDS

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Page/Page column 34; 35, (2015/10/05)

The invention provides compounds and compositions that are useful for treating conditions including Alzheimer's disease, Parkinson's disease, diabetes, cancer, and psychotic disorders such as schizophrenia.

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