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[3-(4-METHOXY-PHENOXY)-PROPYL]-METHYL-AMINE is a chemical compound with the molecular formula C12H19NO2. It is a propyl-methyl-amine derivative featuring a 4-methoxy-phenoxy group attached to the propyl chain. [3-(4-METHOXY-PHENOXY)-PROPYL]-METHYL-AMINE is known for its versatile structure and properties, making it a valuable tool in the pharmaceutical industry and organic synthesis.

303104-76-9

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303104-76-9 Usage

Uses

Used in Pharmaceutical Industry:
[3-(4-METHOXY-PHENOXY)-PROPYL]-METHYL-AMINE is used as a building block for the synthesis of various drug molecules. Its unique structure and properties contribute to the development of new pharmaceuticals and biologically active compounds.
Used in Organic Synthesis:
[3-(4-METHOXY-PHENOXY)-PROPYL]-METHYL-AMINE is also utilized in organic synthesis, where it serves as a key component in the creation of complex organic molecules.
Used in Medicinal Chemistry:
[3-(4-METHOXY-PHENOXY)-PROPYL]-METHYL-AMINE has been studied for its potential applications in medicinal chemistry, where it may play a role in the design and synthesis of novel therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 303104-76-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,3,1,0 and 4 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 303104-76:
(8*3)+(7*0)+(6*3)+(5*1)+(4*0)+(3*4)+(2*7)+(1*6)=79
79 % 10 = 9
So 303104-76-9 is a valid CAS Registry Number.
InChI:InChI=1/C11H17NO2/c1-12-8-3-9-14-11-6-4-10(13-2)5-7-11/h4-7,12H,3,8-9H2,1-2H3

303104-76-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(4-methoxyphenoxy)-N-methylpropan-1-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:303104-76-9 SDS

303104-76-9Relevant academic research and scientific papers

Improved model of lanosterol 14α-demethylase by ligand-supported homology modeling: Validation by virtual screening and azole optimization

Sheng, Chunquan,Wang, Wenya,Che, Xiaoying,Dong, Guoqiang,Wang, Shengzheng,Ji, Haitao,Miao, Zhenyuan,Yao, Jianzhong,Zhang, Wannian

experimental part, p. 390 - 397 (2010/11/18)

Lanosterol 14α-demethylase (CYP51) is an important target for antifungal drugs. An improved three-dimensional model of CYP51 from Candida albicans (CACYP51) was constructed by ligand-supported homology modeling and molecular dynamics simulations. The accuracy of the constructed model was evaluated by its performance in a small-scale virtual screen. The results show that known CYP51 inhibitors were efficiently discriminated by the model, and it performed better than our previous CACYP51 model. The active site of CACYP51 was characterized by multiple copy simultaneous search (MCSS) calculations. On the basis of the MCSS results, a series of novel azoles were designed and synthesized, and they showed good in vitro antifungal activity with a broad spectrum. The MIC80 value of four of these compounds against C. albicans is 0.001 μgmL-1, indicating that they are promising leads for the discovery of novel antifungal agents.

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