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3-[(4-methoxyphenyl)methylene]-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one is a complex organic compound that belongs to the class of organic compounds known as phenylpropanoids and polyketides. This category of molecules includes a wide variety of natural substances derived from phenylalanine or polyketide, having a diverse range of medicinal properties. The methoxy group attached to the phenyl ring suggests the compound may have some level of polarity and potential interaction with a range of biological systems. The particular chemical, given its bicyclic structure, is likely to have significant interactions with biological systems, giving it potential relevance in pharmaceutical or medicinal contexts.

38102-63-5

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38102-63-5 Usage

Uses

Used in Pharmaceutical Industry:
3-[(4-methoxyphenyl)methylene]-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one is used as a potential pharmaceutical compound for its possible interactions with biological systems due to its methoxy group and bicyclic structure.
Used in Medicinal Chemistry Research:
3-[(4-methoxyphenyl)methylene]-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one is used as a subject of study in medicinal chemistry to explore its potential properties and applications in the development of new drugs and therapies.

Check Digit Verification of cas no

The CAS Registry Mumber 38102-63-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,1,0 and 2 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 38102-63:
(7*3)+(6*8)+(5*1)+(4*0)+(3*2)+(2*6)+(1*3)=95
95 % 10 = 5
So 38102-63-5 is a valid CAS Registry Number.
InChI:InChI=1/C18H22O2/c1-17(2)15-9-10-18(17,3)16(19)14(15)11-12-5-7-13(20-4)8-6-12/h5-8,11,15H,9-10H2,1-4H3

38102-63-5SDS

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 2-[(4-methoxyphenyl)methylidene]-4,7,7-trimethylbicyclo[2.2.1]heptan-3-one

1.2 Other means of identification

Product number -
Other names Anisilyden-campher

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:38102-63-5 SDS

38102-63-5Downstream Products

38102-63-5Relevant academic research and scientific papers

RuCl2(DMSO)4 catalyzes the β-alkylation of secondary alcohols with primary alcohols through a hydrogen autotransfer process

Martínez, Ricardo,Ramón, Diego J.,Yus, Miguel

, p. 8982 - 8987 (2007/10/03)

The electrophilic β-alkylation of secondary alcohols with primary alcohols is accomplished by a hydrogen autotransfer process catalyzed by RuCl2(DMSO)4. The reaction can produce either simple alkylated secondary alcohols or α,β-unsaturated ketones with good to excellent results just by choosing the appropriate starting secondary alcohol (methyl or longer chain secondary alcohol, respectively), as well as quinolines (by using 2-aminobenzyl alcohol).

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