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4165-61-1

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4165-61-1 Usage

Description

ANILINE D5, also known as deuterated aniline, is a chemical compound that is a derivative of aniline with deuterium atoms incorporated into its structure. It is commonly used as an internal standard in analytical chemistry for the quantification of aniline.
Used in Analytical Chemistry:
ANILINE D5 is used as an internal standard for the quantification of aniline by gas chromatography (GC) or liquid chromatography (LC) mass spectrometry. Its incorporation of deuterium atoms provides a distinct mass difference from the native aniline, allowing for accurate and precise measurements in the analysis of aniline concentrations in various samples.

Check Digit Verification of cas no

The CAS Registry Mumber 4165-61-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,1,6 and 5 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 4165-61:
(6*4)+(5*1)+(4*6)+(3*5)+(2*6)+(1*1)=81
81 % 10 = 1
So 4165-61-1 is a valid CAS Registry Number.
InChI:InChI=1/C6H7N/c7-6-4-2-1-3-5-6/h1-5H,7H2/i1D,2D,3D,4D,5D

4165-61-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3,4,5,6-pentadeuterioaniline

1.2 Other means of identification

Product number -
Other names Aniline-d5

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:4165-61-1 SDS

4165-61-1Relevant articles and documents

INELASTIC NEUTRON SCATTERING STUDIES OF ETHYLENE-CONTAINING SQUARE PLANAR PLATINUM COMPLEXES

Howard, Joseph,Robson, Keith,Waddington, Thomas C.

, p. 903 - 912 (1982)

The low frequency (0-850 cm-1) modes of vibration of the complexes trans-PtCl2(C2H4)*L (where L=ND3, CD3CN, DCON(CD3)2 and C6D5ND2) and cis-PtCl2(C2H4)*(CD3)2SO have been studied by inelastic neutron scattering, i.r. and Raman spectroscopy.In all complexes, motions of the C2H4 moiety relative to the platinum atom (including torsional modes) have been assigned and the barrier to rotation of the C2H4 ligand about an axis projected from the platinum atom through the centre of the C=C bond determined.The barriers thus calculated have been compared with energies of activation obtained from nuclear magnetic resonance studies of similar complexes.

Maquestiau et al.

, p. 518,525 (1978)

Scalable and selective deuteration of (hetero)arenes

Bartling, Stephan,Beller, Matthias,Bourriquen, Florian,Brückner, Angelika,Junge, Kathrin,Kreyenschulte, Carsten,Lei, Aiwen,Li, Wu,Lund, Henrik,Rabeah, Jabor,Rockstroh, Nils,Surkus, Annette-Enrica,Yang, Dali

, (2022/01/19)

Isotope labelling, particularly deuteration, is an important tool for the development of new drugs, specifically for identification and quantification of metabolites. For this purpose, many efficient methodologies have been developed that allow for the small-scale synthesis of selectively deuterated compounds. Due to the development of deuterated compounds as active drug ingredients, there is a growing interest in scalable methods for deuteration. The development of methodologies for large-scale deuterium labelling in industrial settings requires technologies that are reliable, robust and scalable. Here we show that a nanostructured iron catalyst, prepared by combining cellulose with abundant iron salts, permits the selective deuteration of (hetero)arenes including anilines, phenols, indoles and other heterocycles, using inexpensive D2O under hydrogen pressure. This methodology represents an easily scalable deuteration (demonstrated by the synthesis of deuterium-containing products on the kilogram scale) and the air- and water-stable catalyst enables efficient labelling in a straightforward manner with high quality control. [Figure not available: see fulltext.].

Benzocarbazole Synthesis via Visible-Light-Accelerated Rh(III)-Catalyzed C-H Annulation of Aromatic Amines with Bicyclic Alkenes

Wang, Yichun,Jia, Deyang,Zeng, Jing,Liu, Yuming,Bu, Xiubin,Yang, Xiaobo

, p. 7740 - 7745 (2021/10/20)

A visible-light-accelerated Rh(III)-catalyzed C-H annulation of aromatic amines with bicyclic alkenes for the synthesis of benzocarbazole derivatives was developed. In this approach, with the cooperation of rhodium catalysis and visible-light irradiation, various aromatic amines reacted with oxabicyclic alkenes and azabicyclic alkenes smoothly at room temperature, delivering the corresponding bridged oxa or aza tetrahydro benzocarbazoles in good to excellent yields. Moreover, a series of benzo[b]carbazoles were synthesized conveniently through further aromatization in one pot. The potential of this method was demonstrated via directing-group removal, derivatization, a scale-up reaction, and fluorescence investigations.

Novel organic compounds for organic light-emitting diode and organic light-emitting diode including the same

-

Paragraph 0544-0549, (2020/08/29)

The present invention relates to an organic light emitting compound represented by formula A and an organic light emitting diode including the same. Substituents A1 to A4, R1 to R17, X, Y, a, b, m, n, p, L1, and L2 are identical to as defined in the detailed description.

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