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1065473-05-3

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1065473-05-3 Usage

Description

2-Methoxy-d3-phenol--d4, with the CAS number 1065473-05-3, is an isotopically labeled research compound. It is a derivative of phenol, which is a simple aromatic compound consisting of a hydroxyl (-OH) group bonded directly to a benzene ring. The presence of deuterium (D) in the molecule, a stable isotope of hydrogen, makes it particularly useful for various research applications, including studying the behavior of molecules in biological systems and as a reference in analytical chemistry.

Uses

Used in Research and Development:
2-Methoxy-d3-phenol--d4 is used as a research compound for [application reason] in the field of [application type]. The presence of deuterium in the molecule allows for the study of its behavior in various chemical and biological processes, providing valuable insights into the mechanisms of action and potential applications of similar compounds.
Used in Analytical Chemistry:
In the field of analytical chemistry, 2-Methoxy-d3-phenol--d4 is used as a reference compound for [application reason]. Its isotopically labeled nature makes it an ideal candidate for calibration and validation of analytical instruments, ensuring accurate and reliable measurements in various chemical analyses.
Used in Pharmaceutical Research:
2-Methoxy-d3-phenol--d4 is also used as a pharmaceutical research compound for [application reason]. Its unique properties and deuterium labeling make it a valuable tool in the development of new drugs and the study of their interactions with biological targets.
Used in Chemical Synthesis:
In the chemical synthesis industry, 2-Methoxy-d3-phenol--d4 is used as a starting material or intermediate for [application reason]. Its deuterium labeling can provide insights into the reaction mechanisms and help optimize the synthesis of complex molecules with potential applications in various fields, such as pharmaceuticals, agrochemicals, and materials science.
Used in Environmental Studies:
2-Methoxy-d3-phenol--d4 is employed as a tracer compound in environmental studies for [application reason]. Its isotopically labeled nature allows researchers to track the fate and transport of phenolic compounds in the environment, providing valuable information on their behavior, degradation, and potential impact on ecosystems.
Used in Material Science:
In the field of material science, 2-Methoxy-d3-phenol--d4 is used as a component in the development of advanced materials for [application reason]. Its unique properties and deuterium labeling can contribute to the design and synthesis of novel materials with enhanced performance characteristics, such as improved stability, reactivity, or selectivity.

Check Digit Verification of cas no

The CAS Registry Mumber 1065473-05-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,6,5,4,7 and 3 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1065473-05:
(9*1)+(8*0)+(7*6)+(6*5)+(5*4)+(4*7)+(3*3)+(2*0)+(1*5)=143
143 % 10 = 3
So 1065473-05-3 is a valid CAS Registry Number.

1065473-05-3SDS

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 d7-2-methoxyphenol

1.2 Other means of identification

Product number -
Other names d7-guaiacol

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:1065473-05-3 SDS

1065473-05-3Relevant articles and documents

Aqueous Oxidations Started by TiO2 Photoinduced Holes Can Be a Rate-Determining Step

Gong, Yuanzheng,Yang, Chun,Ji, Hongwei,Chen, Chuncheng,Ma, Wanhong,Zhao, Jincai

supporting information, p. 2048 - 2051 (2017/08/23)

In aqueous TiO2 photocatalytic hydroxylation of weakly polar aromatics, a series of inverse H/D KIEs of 0.7–0.8 were observed, which is different than the normal H/D kinetic isotope effects (KIEs) usually observed for polar aromatics. This result indicated that the oxidation started by photo-induced hvb + can be the rate-determining step.

SUBSTITUTED PYRIMIDINES

-

Page/Page column 38-39, (2008/12/07)

Disclosed herein are substituted pyrimidine-based endothelin modulators of Formula I, processes of preparation thereof, pharmaceutical compositions thereof, and methods of use thereof.

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