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92050-16-3

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  • Factory Price OLED 99% 92050-16-3 5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthylamine Manufacturer

    Cas No: 92050-16-3

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92050-16-3 Usage

General Description

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 with the molecular formula C16H25N. It is an amine derivative and a member of the amine family. 5,5,8,8-Tetramethyl-5,6,7,8-tetrahydronaphthalen-2-ylamine has a unique molecular structure, with a tetramethyl substitution on the aromatic ring and a tetrahydronaphthalen-2-ylamine moiety. It has potential applications in pharmaceuticals and medicinal chemistry due to its structural features. 5,5,8,8-Tetramethyl-5,6,7,8-tetrahydronaphthalen-2-ylamine can be synthesized through various synthetic routes and may have potential biological activity that could be of interest for further research and development.

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

92050-16-3Relevant articles and documents

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

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.

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