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(E)-1-(7-methyl-2,3-dihydro-1H-inden-4-yl)-1-(naphthalen-1-yl)methanimine hydrochloride (1:1) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

63549-35-9

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63549-35-9 Usage

Uses

Used in Pharmaceutical Industry:
(E)-1-(7-methyl-2,3-dihydro-1H-inden-4-yl)-1-(naphthalen-1-yl)methanimine hydrochloride (1:1) is used as a potential active pharmaceutical ingredient (API) for the development of new drugs due to its unique molecular structure and potential biological activity. Its specific application may be determined through further research and development, as it could potentially target various biological pathways or receptors.
Used in Research and Development:
In the field of research and development, (E)-1-(7-methyl-2,3-dihydro-1H-inden-4-yl)-1-(naphthalen-1-yl)methanimine hydrochloride (1:1) is used as a chemical probe for studying the interactions of various biological targets. Its unique structure may allow researchers to gain insights into the mechanisms of action of certain diseases or conditions, potentially leading to the discovery of novel therapeutic approaches.
Used in Chemical Synthesis:
(E)-1-(7-methyl-2,3-dihydro-1H-inden-4-yl)-1-(naphthalen-1-yl)methanimine hydrochloride (1:1) may also be used as a synthetic intermediate or building block in the synthesis of more complex organic compounds. Its double bond and functional groups could be exploited in various chemical reactions to produce a range of different molecules with potential applications in various industries, including pharmaceuticals, materials science, and agrochemicals.
Used in Material Science:
In the field of material science, (E)-1-(7-methyl-2,3-dihydro-1H-inden-4-yl)-1-(naphthalen-1-yl)methanimine hydrochloride (1:1) could be explored for its potential to contribute to the development of new materials with specific properties. Its molecular structure may allow for the creation of materials with unique optical, electronic, or mechanical characteristics, which could be useful in various applications, such as in the development of advanced sensors, displays, or energy storage devices.

Check Digit Verification of cas no

The CAS Registry Mumber 63549-35-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,5,4 and 9 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 63549-35:
(7*6)+(6*3)+(5*5)+(4*4)+(3*9)+(2*3)+(1*5)=139
139 % 10 = 9
So 63549-35-9 is a valid CAS Registry Number.

63549-35-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(7-Methyl-4-indanyl)-1-(1-naphthyl)methanimine, hydrochloride

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

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

More Details:63549-35-9 SDS

63549-35-9Relevant academic research and scientific papers

Improved Synthesis of 3-Methylcholanthrene

Tang, Ping Wah,Maggiulli, Cataldo A.

, p. 3429 - 3432 (2007/10/02)

An improved synthesis of 7-methylindan-4-yl 1-naphthyl ketone (3), an important precursor of 3-methylcholanthrene (1), has been developed.The key intermediates for 3, 4-cyano-7-methylindan (2a) and 4-(ethoxycarbonyl)-7-methylindan (2b), were conveniently prepared in high yields by reaction of 1-(1-pyrrolidino)cyclopentene (6) with sorbonitrile (5a) or ethyl sorbate (5b), followed by aromatization with sulfur. 1-Naphthylmagnesium bromide (4b) in the presence of cuprous iodide reacted cleanly with 4-(chloromethanoyl)-7-methylindan (12) to give 3.The Friedel-Crafts acylation of naphthalene with 12 afforded 84percent of 3 and 16percent of β isomer 13.Alternatively, 3 was prepared in 75percent yield by condensation of Grignard reagent 4b with 2a in THF.Thermal annelation of 3 afforded 1 in 41.5percent yield.

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