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70026-36-7

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70026-36-7 Usage

Description

PHENYL-D5-ACETONITRILE, also known as Labelled Benzeneacetonitrile, is a volatile compound that is released from apple trees infested with Light brown apple moth larvae. It is a derivative of acetonitrile with a phenyl group attached, and the D5 label indicates that it has five deuterium atoms replacing hydrogen atoms in the molecule. PHENYL-D5-ACETONITRILE is of interest due to its potential use in various applications, particularly in the field of chemical ecology and pest management.

Uses

Used in Chemical Ecology:
PHENYL-D5-ACETONITRILE is used as a chemical marker for the detection of Light brown apple moth larvae infestations in apple trees. The presence of this compound can indicate the presence of the pest, allowing for timely intervention and management strategies to protect the apple crop.
Used in Pest Management:
PHENYL-D5-ACETONITRILE is used as a tool in the development of pest management strategies for apple growers. By understanding the chemical signatures of infested trees, growers can implement targeted control measures to reduce the impact of the Light brown apple moth on their crops.
Used in Research and Development:
PHENYL-D5-ACETONITRILE is used as a research compound to study the chemical communication and behavior of the Light brown apple moth. This knowledge can contribute to the development of novel pest control methods, such as pheromone-based traps or other biocontrol strategies.
Used in Analytical Chemistry:
PHENYL-D5-ACETONITRILE can be used as an internal standard or reference compound in analytical chemistry, particularly in the analysis of volatile organic compounds in the environment or in the study of plant-pest interactions. Its unique properties and stable isotopic labeling make it a valuable tool for accurate quantification and identification of target compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 70026-36-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,0,2 and 6 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 70026-36:
(7*7)+(6*0)+(5*0)+(4*2)+(3*6)+(2*3)+(1*6)=87
87 % 10 = 7
So 70026-36-7 is a valid CAS Registry Number.

70026-36-7SDS

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 2-(2,3,4,5,6-pentadeuteriophenyl)acetonitrile

1.2 Other means of identification

Product number -
Other names pentadeuteriophenylacetonitrile

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:70026-36-7 SDS

70026-36-7Relevant articles and documents

Synthesis of stable isotope-labeled nasturlexins and potential precursors to probe biosynthetic pathways of cruciferous phytoalexins

Pedras, M. Soledade C.,To, Q. Huy

, p. 94 - 106 (2018/02/09)

The syntheses of perdeuterated phytoalexins nasturlexins A and C, and putative biosynthetic precursors, including phenylethyl isothiocyanates and phenylethyl dithiocarbamates, using commercially available [2,3,4,5,6-D5]phenylalanine, [2,3,4,5,6

Synthesis of indolines by copper-mediated intramolecular aromatic C-H amination

Takamatsu, Kazutaka,Hirano, Koji,Satoh, Tetsuya,Miura, Masahiro

, p. 3242 - 3249 (2015/03/30)

A Cu(OAc)2-mediated intramolecular aromatic C-H amination proceeds with the aid of a picolinamide-type bidentate coordination group to deliver the corresponding indolines in good yields. The reaction occurs smoothly even under noble-metal-free conditions, and in some cases the use of an MnO2 terminal oxidant renders the process catalytic in Cu. The mild oxidation aptitude of Cu(OAc)2 and/or MnO2 accommodates the formation of electron-rich thiophene-and indole-fused indoline analogues. The Cu-based system can provide an effective approach to various indolines of potent interest in pharmaceutical and medicinal chemistry.

Photolysis of alkylhalodiazirines and direct observation of benzylchlorocarbene in cryogenic matrices

Wierlacher, Stefan,Sander, Wolfram,Uu, Michael T. H.

, p. 8943 - 8953 (2007/10/02)

Photolysis of 3-benzyl-3-chlorodiazirine and its deuterated homologues 3-chloro-3-(phenyldideuteriomethyl)diazirine and 3-chloro-3-((pentadeuteriophenyl)methyl)diazirine has been investigated by means of IR and UV-vis spectroscopy in argon and xenon matri

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