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52670-38-9

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52670-38-9 Usage

General Description

2-Ethynylaniline 98 is a chemical compound with the molecular formula C8H7N. It is a white to light brown solid at room temperature with a melting point of around 112-114°C. 2-ETHYNYLANILINE 98 is primarily used as an intermediate in the production of various dyes and pigments. It can also be used as a building block in the synthesis of pharmaceuticals and agrochemicals. Additionally, 2-Ethynylaniline 98 is a versatile reagent in organic synthesis, and it can undergo various chemical reactions to form different derivatives for different applications. As a chemical, it should be handled and stored with proper care, as it may pose hazards to human health and the environment if not managed appropriately.

Check Digit Verification of cas no

The CAS Registry Mumber 52670-38-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,6,7 and 0 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 52670-38:
(7*5)+(6*2)+(5*6)+(4*7)+(3*0)+(2*3)+(1*8)=119
119 % 10 = 9
So 52670-38-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H7N/c1-2-7-5-3-4-6-8(7)9/h1,3-6H,9H2

52670-38-9 Well-known Company Product Price

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  • Aldrich

  • (597651)  2-Ethynylaniline  98%

  • 52670-38-9

  • 597651-1G

  • 787.41CNY

  • Detail
  • Aldrich

  • (597651)  2-Ethynylaniline  98%

  • 52670-38-9

  • 597651-5G

  • 2,698.02CNY

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52670-38-9SDS

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-ethynylaniline

1.2 Other means of identification

Product number -
Other names O-AMINOPHENYLACETYLENE

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:52670-38-9 SDS

52670-38-9Relevant articles and documents

Divergent Carbocatalytic Routes in Oxidative Coupling of Benzofused Heteroaryl Dimers: A Mechanistic Update

Casadio, David S.,Aikonen, Santeri,Lenarda, Anna,Nieger, Martin,Hu, Tao,Taubert, Stefan,Sundholm, Dage,Muuronen, Mikko,Wirtanen, Tom,Helaja, Juho

supporting information, p. 5283 - 5291 (2021/02/26)

Mildly thermal air or HNO3 oxidized activated carbons catalyse oxidative dehydrogenative couplings of benzo[b]fused heteroaryl 2,2’-dimers, e.g., 2-(benzofuran-2-yl)-1H-indole, to chiral 3,3’-coupled cyclooctatetraenes or carbazole-type migrative products under O2 atmosphere. DFT calculations show that the radical cation and the Scholl-type arenium cation mechanisms lead to different products with 2-(benzofuran-2-yl)-1H-indole, being in accord with experimental product distributions.

Metal-free cascade boron–heteroatom addition and alkylation with diazo compounds

Lv, Jiahang,Zhao, Binlin,Han, Ying,Yuan, Yu,Shi, Zhuangzhi

supporting information, p. 691 - 694 (2020/07/13)

Transition metal-catalyzed carbene transfer reaction is one of the most notable advances for C?C bond formation reactionsduring the past decade, which has been widely employed in the preparation of C3-substituted indoles. Here, we described an efficient e

New indolo[1,2-c]quinazolines for single-crystal field-effect transistor: A united experimental and theoretical studies

Puli, Venkat Swamy,Kilaru, Suresh,Bhongiri, Yadagiri,Marri, Sreenath Reddy,Tripathi, Anuj,Chetti, Prabhakar,Chatterjee, Anindita,Vukoti, Kiran Kumar,Pola, Someshwar

, (2021/08/30)

Here, we account the synthesis and characterization of a series of symmetrical fused heterocyclic aromatic hydrocarbons (HAHs) with an indolo[1,2-c]quinazoline (IQ) as the core moiety. All the new HAHs IQ series were systematically investigated by using various spectroscopic methods. Furthermore, their photo-physical properties were supported by density functional theory (DFT) and time-dependent density functional theory (TDDFT) studies to support the experimental findings. The tetramethyl-substituted indolo[1,2-c]quinazoline (TMIQ) compound is shown to exhibit the shifted type of π–π stacking interactions, which render this series as a new semiconducting material. Single-crystal-based field-effect transistor devices of TMIQ exhibited efficient charge transport behavior, giving a p-channel field-effect mobility of 0.25 cm2?V?1?s?1 with an on/off ratio of 5 × 105.

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