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6-Ethyl-2-tetralone, a bicyclic ketone with the molecular formula C14H16O, is a pale yellow liquid characterized by its sweet, floral odor. It serves as a key intermediate in the synthesis of a variety of biologically active compounds, including pharmaceuticals and fragrances. Its versatile reactivity and functional groups make it a valuable building block in organic chemistry, often used as a starting material for the preparation of other organic compounds such as alkaloids and steroids.

37436-25-2

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37436-25-2 Usage

Uses

Used in Pharmaceutical Industry:
6-Ethyl-2-tetralone is used as a precursor in the production of pharmaceuticals for its ability to be synthesized into various biologically active compounds, contributing to the development of new medications.
Used in Fragrance Industry:
It is utilized as a key intermediate in the creation of fragrances, capitalizing on its sweet, floral scent to enhance the olfactory profiles of various perfumes and scented products.
Used in Organic Synthesis:
6-Ethyl-2-tetralone is employed as a starting material in the preparation of other organic compounds, such as alkaloids and steroids, due to its versatile reactivity and functional groups, which make it an essential building block in organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 37436-25-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,4,3 and 6 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 37436-25:
(7*3)+(6*7)+(5*4)+(4*3)+(3*6)+(2*2)+(1*5)=122
122 % 10 = 2
So 37436-25-2 is a valid CAS Registry Number.

37436-25-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-ethyl-3,4-dihydro-1H-naphthalen-2-one

1.2 Other means of identification

Product number -
Other names 6-Aethyl-2-tetralon

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:37436-25-2 SDS

37436-25-2Downstream Products

37436-25-2Relevant academic research and scientific papers

Synthesis method of Alectinib

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, (2016/10/10)

The invention discloses a synthesis method of Alectinib. The method comprises the following steps: carrying out a borating reaction between 6-bromo-3,4-dihydro-2-naphthalenone and n-butyl lithium and then an organic boron reagent; carrying out a catalytic coupling reaction between the obtained 3,4,-dihydro-2-naphthalenone-6-boric acid and bromoethane; carrying out a dimethylation reaction between the obtained 6-ethyl-3,4-dihydro-2-naphthalenone and iodomethane; carrying out a bromination reaction between the obtained 1,1-dimethyl-6-ethyl-3,4-dihydro-2-naphthalenone and a bromination reagent; carrying out a substitution reaction between the obtained 1,1-dimethyl-6-ethyl-7-bromo-3,4-dihydro-2-naphthalenone and 4-(4-piperidyl)morpholine; carrying out a cyclization reaction between the obtained 1,1-dimethyl-6-ethyl-7-[4-(morpholine-4-yl)piperidine-1-yl]-3,4-dihydro-2-naphthalenone and 3-cyanophenylhydrazine; and carrying out an oxidation reaction between the obtained 9-ethyl-6,6-dimethyl-8-[4-(morpholine-4-yl)piperidine-1-yl]-6,11-dihydro-5H-benzo[b]carbazole-3-formonitrile and dichlorodicyanobenzoquinone to obtain a finished product of Alectinib. The synthesis method has the advantages of relatively short route, simplified operation and relatively low cost and is a green and environment-friendly method suitable for industrial production.

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