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4-Chloro-6-nitrosoresorcinol-13C6, with the chemical formula C7(13C6)H4ClNO2, is a stable isotope-labeled compound derived from 4-chloro-6-nitrosoresorcinol. It incorporates six 13C atoms in its structure, which makes it a valuable tool in various scientific and industrial applications. 4-Chloro-6-nitrosoresorcinol-13C6 is characterized by its unique properties, such as its molecular weight and reactivity, which are influenced by the presence of the 13C isotope.

953390-33-5

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953390-33-5 Usage

Uses

Used in Organic Synthesis:
4-Chloro-6-nitrosoresorcinol-13C6 is used as a synthetic building block in organic synthesis for the preparation of various organic compounds. The incorporation of 13C atoms allows for the tracking and analysis of the compound's behavior during chemical reactions, providing valuable insights into reaction mechanisms and pathways.
Used in Chemical Research:
In the field of chemical research, 4-Chloro-6-nitrosoresorcinol-13C6 serves as a valuable tracer compound. Its use in isotope labeling enables researchers to study the dynamics of chemical reactions, including reaction rates, intermediates, and product formation, with enhanced precision and accuracy.
Used in Pharmaceutical Industry:
4-Chloro-6-nitrosoresorcinol-13C6 is used as a key intermediate in the synthesis of pharmaceutical compounds. Its unique properties and stable isotope labeling make it an attractive candidate for the development of new drugs and drug candidates, as well as for the improvement of existing ones.
Used in Environmental Studies:
In environmental studies, 4-Chloro-6-nitrosoresorcinol-13C6 can be employed as a tracer to monitor the fate and transport of pollutants in the environment. The use of 13C-labeled compounds allows for the differentiation between naturally occurring and anthropogenic sources of contaminants, providing valuable information for environmental management and remediation efforts.
Used in Analytical Chemistry:
4-Chloro-6-nitrosoresorcinol-13C6 is used as an internal standard in analytical chemistry for the quantification and identification of related compounds. Its stable isotopic composition ensures accurate measurements and reliable results, making it a valuable tool in various analytical techniques, such as mass spectrometry and nuclear magnetic resonance (NMR) spectroscopy.

Check Digit Verification of cas no

The CAS Registry Mumber 953390-33-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,3,3,9 and 0 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 953390-33:
(8*9)+(7*5)+(6*3)+(5*3)+(4*9)+(3*0)+(2*3)+(1*3)=185
185 % 10 = 5
So 953390-33-5 is a valid CAS Registry Number.
InChI:InChI=1/C6H4ClNO3/c7-3-1-4(8-11)6(10)2-5(3)9/h1-2,9-10H/i1+1,2+1,3+1,4+1,5+1,6+1

953390-33-5SDS

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 4-chloro-6-nitrosobenzene-1,3-diol

1.2 Other means of identification

Product number -
Other names 4-Chloro-6-nitroso-1,3-benzenediol-1,2,3,4,5,6-13C6

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:953390-33-5 SDS

953390-33-5Upstream product

953390-33-5Downstream Products

953390-33-5Relevant academic research and scientific papers

An improved synthesis of isotope labeled 6-hydroxychlorzoxazone

Jian, Zhigang,Ray, Tapan,Wu, Amy,Jones, Lawrence

, p. 979 - 984 (2006)

[13C6]6-Hydroxychlorzoxazone, a major P450 metabolite of chlorzoxazone, was synthesized from [13C6]benzene in an overall 18% yield. An improved procedure for converting 4-chloro-6- nitrosoresorcinol to 6-hydroxy

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