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287399-32-0

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287399-32-0 Usage

Description

ETHYL-1-13C-BENZENE 99 ATOM % 13C, also known as Ethyl-alpha-13C-benzene (CAS# 287399-32-0), is an isotopically labeled research compound. It is a variant of ethylbenzene with a 13C atom replacing one of the 12C atoms in the benzene ring, which makes it a valuable tool for various research applications.

Uses

Used in Research and Development:
ETHYL-1-13C-BENZENE 99 ATOM % 13C is used as a research compound for studying the behavior and properties of molecules in various chemical and biological processes. The presence of the 13C atom allows for easier tracking and analysis of the compound within complex systems, making it a valuable tool for researchers.
Used in Chemical Reactions:
In the field of organic chemistry, ETHYL-1-13C-BENZENE 99 ATOM % 13C is used as a reactant or a starting material for the synthesis of other isotopically labeled compounds. The 13C labeling can help in understanding reaction mechanisms and determining the position of the labeled atom in the final product.
Used in Analytical Techniques:
ETHYL-1-13C-BENZENE 99 ATOM % 13C is used as a reference material in various analytical techniques, such as mass spectrometry and nuclear magnetic resonance (NMR) spectroscopy. The 13C labeling provides a distinct signature that can be used to calibrate instruments and improve the accuracy of measurements.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, ETHYL-1-13C-BENZENE 99 ATOM % 13C can be used as a building block for the synthesis of isotopically labeled drug candidates. These labeled compounds can be used in preclinical and clinical studies to investigate the pharmacokinetics, metabolism, and toxicity of the drug.
Used in Environmental Studies:
ETHYL-1-13C-BENZENE 99 ATOM % 13C can be employed in environmental studies to trace the fate and transport of ethylbenzene and its derivatives in the environment. The 13C labeling can help in distinguishing between natural and anthropogenic sources of the compound, providing valuable insights into its environmental impact.

Check Digit Verification of cas no

The CAS Registry Mumber 287399-32-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,8,7,3,9 and 9 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 287399-32:
(8*2)+(7*8)+(6*7)+(5*3)+(4*9)+(3*9)+(2*3)+(1*2)=200
200 % 10 = 0
So 287399-32-0 is a valid CAS Registry Number.

287399-32-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethyl-1-13C-benzene

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

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:287399-32-0 SDS

287399-32-0Upstream product

287399-32-0Relevant articles and documents

Thermal isomerization of benzocyclobutene

Chapman, Orville L.,Tsou, Uh-Po Eric,Johnson, Jeffery W.

, p. 553 - 559 (2007/10/02)

Thermolysis of benzocyclobutene 13CH2, 99percent gives styrene labeled in the β (48percent), ortho (30percent), α (14percent), meta (4percent), and para (4percent) positions.The major labels (β and ortho) are consistent with a mechanism involving interconversions of the isomeric tolylmethylenes and the methylcycloheptatrienes.This mechanism also involves interconversion of o-tolylmethylene with o-xylylene and p-tolylmethylene with p-xylylene.A minor mechanism produces 25percent of styrene.This mechanism involves cleavage of the aryl carbon to the methylene carbon bond in benzocyclobutene followed by hydrogen transfer to produce styrene.Thermolysis of p-xylylene produced from paracyclophane gives styrene (55percent), p-xylene (31percent), benzocyclobutene (4percent), benzene (4percent), and toluene (3percent).Thermolysis of metacyclophane gives styrene (18percent), p-xylene (25percent), m-xylene (3percent), benzocyclobutene (1percent), benzene (7percent), and toluene (22percent).

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