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1021126-94-2

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1021126-94-2 Usage

General Description

"(4-methoxy-3-phenethoxyphenyl)methanol" is a chemical compound with the molecular formula C16H18O3. It is a derivative of phenol, containing a methoxy group and a phenethoxy group. (4-methoxy-3-phenethoxyphenyl)methanol has potential applications in the pharmaceutical industry, with studies showing its potential as an anti-inflammatory and analgesic agent. Additionally, it may also have uses in the synthesis of other organic compounds due to its unique structure. As with any chemical compound, proper handling and safety precautions should be taken when working with "(4-methoxy-3-phenethoxyphenyl)methanol" to avoid any potential hazards.

Check Digit Verification of cas no

The CAS Registry Mumber 1021126-94-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,1,1,2 and 6 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1021126-94:
(9*1)+(8*0)+(7*2)+(6*1)+(5*1)+(4*2)+(3*6)+(2*9)+(1*4)=82
82 % 10 = 2
So 1021126-94-2 is a valid CAS Registry Number.

1021126-94-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name [4-methoxy-3-(2-phenylethoxy)phenyl]methanol

1.2 Other means of identification

Product number -
Other names (4-methoxy-3-phenethoxyphenyl)methanol

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:1021126-94-2 SDS

1021126-94-2Relevant articles and documents

Design, synthesis, structure-activity relationships, and biological characterization of novel arylalkoxyphenylalkylamine σ ligands as potential antipsychotic drugs

Nakazato, Atsuro,Ohta, Kohmei,Sekiguchi, Yoshinori,Okuyama, Shigeru,Chaki, Shigeyuki,Kawashima, Yutaka,Hatayama, Katsuo

, p. 1076 - 1087 (2007/10/03)

Receptor antagonists may be effective antipsychotic drugs that do not induce motor side effects caused by ingestion of classical drugs such as haloperidol. We obtained evidence that 1-(2-dipropylaminoethyl)-4-methoxy- 6H-dibenzo[b,d]pyran hydrochloride 2a had selective affinity for σ receptor over dopamine D2 receptor. This compound was designed to eliminate two bonds of apomorphine 1 to produce structural flexibility for the nitrogen atom and to bridge two benzene rings with a -CH2O- bond to maintain the planar structure. In light of the evidence, N,Y-dipropyl-2-(4-methoxy-3- benzyloxylphenyl)ethylamine hydrochloride 10b was designed. Since compound 10b had eliminated a biphenyl bond of 6H-dibenzo[b,d]pyran derivative 2a, it might be more released from the rigid structure of apomorphine 1 than compound 2a. The chemical modification of compound 10b led to the discovery that N,N-dipropyl-2-[4-methoxy-3-(2-phenylethoxyl)phenyl]ethylamine hydrochloride 10g (NE- 100), the best compound among arylalkoxyphenylalkylamine derivatives 3, had a high and selective affinity for σ receptor and had a potent activity in an animal model when the drug was given orally. We report here the design, synthesis, structure-activity relationships, and biological characterization of novel arylalkoxyphenylalkylamine derivatives 3.

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