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METHYL 4-METHOXY-[7-13C]-BENZOATE, with the chemical formula C8H7O3 and a molecular weight of 166.14 g/mol, is a stable isotope-labeled compound where the carbon atom at the 7th position is replaced with 13C. This substitution allows for enhanced tracking and analysis in various chemical and biological processes. It is a white crystalline solid and is soluble in common organic solvents.

93627-95-3

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93627-95-3 Usage

Uses

Used in Organic Synthesis:
METHYL 4-METHOXY-[7-13C]-BENZOATE is used as a synthetic intermediate for the preparation of various organic compounds. Its stable isotope labeling allows for the tracing of metabolic pathways and the elucidation of reaction mechanisms in chemical processes.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, METHYL 4-METHOXY-[7-13C]-BENZOATE is used as a labeled compound for the development of new drugs and the study of drug metabolism. The incorporation of 13C into the molecule enables researchers to monitor the fate of the compound within the body and assess its pharmacokinetics and pharmacodynamics.
Used in Research and Development:
METHYL 4-METHOXY-[7-13C]-BENZOATE is utilized in academic and industrial research settings for the investigation of chemical reactions, the synthesis of novel compounds, and the development of analytical methods. Its stable isotope labeling provides a valuable tool for researchers to study the behavior of molecules in complex systems.
Used in Environmental Studies:
In environmental science, METHYL 4-METHOXY-[7-13C]-BENZOATE can be employed as a tracer compound to study the fate and transport of pollutants in the environment. The 13C labeling allows for the differentiation between the labeled compound and naturally occurring substances, providing insights into the environmental impact of chemicals.
Used in Analytical Chemistry:
METHYL 4-METHOXY-[7-13C]-BENZOATE serves as a reference material in analytical chemistry for the calibration of instruments and the development of new analytical techniques. The stable isotope labeling enhances the sensitivity and accuracy of measurements, particularly in mass spectrometry and nuclear magnetic resonance (NMR) spectroscopy.

Check Digit Verification of cas no

The CAS Registry Mumber 93627-95-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,6,2 and 7 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 93627-95:
(7*9)+(6*3)+(5*6)+(4*2)+(3*7)+(2*9)+(1*5)=163
163 % 10 = 3
So 93627-95-3 is a valid CAS Registry Number.

93627-95-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 4-methoxybenzoate

1.2 Other means of identification

Product number -
Other names 4-Methoxy-benzoic-carboxy-13C Acid Methyl Ester

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:93627-95-3 SDS

93627-95-3Relevant academic research and scientific papers

Palladium-catalyzed carbonylations of aryl bromides using paraformaldehyde: Synthesis of aldehydes and esters

Natte, Kishore,Dumrath, Andreas,Neumann, Helfried,Beller, Matthias

supporting information, p. 10090 - 10094 (2015/03/31)

Carbonylation reactions represent useful tools for organic synthesis. However, the necessity to use gaseous carbon monoxide is a disadvantage for most organic chemists. To solve this problem, novel protocols have been developed for conducting palladium-catalyzed reductive carbonylations of aryl bromides and alkoxycarbonylations using paraformaldehyde as an external CO source (CO gas free). Hence, aromatic aldehydes and esters were synthesized in moderate to good yields.

Studies on the biosynthesis of the antibiotic reductiomycin in Streptomyces xanthochromogenus

Cho,Beale,Graff,Mocek,Nakagawa,Omura,Floss

, p. 12296 - 12304 (2007/10/02)

The biosynthesis of the antibiotic reductiomycin (1) in Streptomyces xanthochromogenus was investigated by feeding experiments with radioactive and stable isotope-labeled precursors. NMR and mass spectroscopic analyses of the labeled 1 samples revealed th

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