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1-NaphthaleneMethanaMine, 7,8-dihydro-α-Methyl-N-[3-[3-(trifluoroMethyl)phenyl]propyl]is a complex chemical compound derived from naphthalenemethanamine, featuring a trifluoromethyl group. 1-NaphthaleneMethanaMine, 7,8-dihydro-α-Methyl-N-[3-[3-(trifluoroMethyl)phenyl]propyl]is characterized by its intricate molecular structure and is utilized in various research and development applications.

802918-46-3

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  • 1-NaphthaleneMethanaMine, 7,8-dihydro-α-Methyl-N-[3-[3-(trifluoroMethyl)phenyl]propyl]-

    Cas No: 802918-46-3

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802918-46-3 Usage

Uses

Used in Pharmaceutical Research and Development:
1-NaphthaleneMethanaMine, 7,8-dihydro-α-Methyl-N-[3-[3-(trifluoroMethyl)phenyl]propyl]is employed as a key intermediate in the synthesis of pharmaceutical compounds. Its unique structure allows it to be a building block for the development of new drugs with potential therapeutic applications.
Used in Agrochemical Research and Development:
In the agrochemical industry, 1-NaphthaleneMethanaMine, 7,8-dihydro-α-Methyl-N-[3-[3-(trifluoroMethyl)phenyl]propyl]is used as a component in the creation of novel agrochemicals. Its properties make it suitable for the development of pesticides, herbicides, and other agricultural chemicals to improve crop protection and yield.
Used in Organic Synthesis:
1-NaphthaleneMethanaMine, 7,8-dihydro-α-Methyl-N-[3-[3-(trifluoroMethyl)phenyl]propyl]is utilized as a versatile reagent in organic synthesis. Its complex structure allows it to be a precursor for the formation of various organic compounds, contributing to the advancement of organic chemistry.
Used in Industrial Applications:
Due to its unique properties, 1-NaphthaleneMethanaMine, 7,8-dihydro-α-Methyl-N-[3-[3-(trifluoroMethyl)phenyl]propyl]may have potential uses in various industrial applications. However, its complex structure and potential hazards require careful consideration and safety precautions to ensure its safe and effective use in these settings.

Check Digit Verification of cas no

The CAS Registry Mumber 802918-46-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,0,2,9,1 and 8 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 802918-46:
(8*8)+(7*0)+(6*2)+(5*9)+(4*1)+(3*8)+(2*4)+(1*6)=163
163 % 10 = 3
So 802918-46-3 is a valid CAS Registry Number.

802918-46-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name [1-(7,8-Dihydro-naphthalen-1-yl)-ethyl]-[3-(3-trifluoromethyl-phenyl)-propyl]-amine

1.2 Other means of identification

Product number -
Other names -

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

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More Details:802918-46-3 SDS

802918-46-3Relevant articles and documents

Efficient synthesis of substances related to cinacalcet hydrochloride via heck coupling

Lei, Fan,Qu, Boyi,Li, Xiaolong,Guo, Li,Guan, Mei,Hai, Li,Jin, Hui,Wu, Yong

, p. 2879 - 2885 (2014/09/29)

Efficient synthetic methods to process substances related to cinacalcet hydrochloride 1, generated during the preparation, were described. The compounds were identified as [1-(7,8-dihydro-naphthalen-1-yl)-ethyl]-[3-(3- trifluoromethyl-phenyl)-propyl]-amine hydrochloride 2,[1-(5,6,7,8-tetrahydro- naphthalen-1-yl)-ethyl]-[3-(3-trifluoromethyl-phenyl)-propyl]-amine hydrochloride 3 and [1-(naphthalen-2-yl)-ethyl]-[3-(3-trifluoromethyl-phenyl)- propyl]-amine hydrochloride 4. All were prepared from commercially available materials in several linear steps and characterized by their respective spectral data.

Synthesis of Cinacalcet congeners

Wang, Xin,Chen, Ying,Crockett, Richard,Briones, Jorge,Yan, Tony,Orihuela, Carlos,Zhi, Benxin,Ng, John

, p. 8355 - 8358 (2007/10/03)

Two related substances 1 and 2 of Cinacalet were prepared. Two racemic isomeric dihydronaphthalenes 1 and 2 were prepared from commercially available 5-hydroxytetralone in five linear steps. A key palladium-catalyzed double bond migration led to the synthesis of both isomers from the same starting material. Preparative chiral HPLC separation provided the enantiomerically pure materials. An asymmetric synthesis employing CBS reduction to furnish 1 was also developed.

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