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84944-75-2

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84944-75-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84944-75-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,9,4 and 4 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 84944-75:
(7*8)+(6*4)+(5*9)+(4*4)+(3*4)+(2*7)+(1*5)=172
172 % 10 = 2
So 84944-75-2 is a valid CAS Registry Number.

84944-75-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3-dihydro-1-benzofuran-5-carbonitrile

1.2 Other means of identification

Product number -
Other names OR0378

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:84944-75-2 SDS

84944-75-2Downstream Products

84944-75-2Relevant articles and documents

A convenient reagent for the conversion of aldoximes into nitriles and isonitriles

Zhang, Wei,Lin, Jin-Hong,Zhang, Pengfei,Xiao, Ji-Chang

supporting information, p. 6221 - 6224 (2020/06/29)

For the dehydroxylation of aldoximes with 4-nitro-1-((trifluoromethyl)sulfonyl)-imidazole (NTSI), slight modifications of reaction conditions resulted in significantly different reaction paths to provide either nitriles or isonitriles. The challenging conversion of aldoximes into isonitriles was achieved under mild conditions.

Synthesis method of benzonitrile compounds

-

Paragraph 0076; 0077; 0078, (2018/04/02)

The invention provides a preparation method of benzonitrile compounds. The preparation method comprises the steps: carrying out a reaction in an organic solvent at 0-50 DEG C for 4-12h under the action of an oxidant by taking phenylacetylene as shown in the formula (I) and a derivative of phenylacetylene as raw materials and nitrite as a nitrogen source, and separating and purifying the obtained reaction liquid to prepare the benzonitrile compound as shown in the formula (II); and the amount-of-substance ratio of the nitrogen source to phenylacetylene as shown in the formula (I) and the derivative of phenylacetylene is (1-3):1. The preparation method is simple and available in raw material, mild in reaction condition, good in functional group tolerance, simple in operation and environment-friendly so as to be a novel method for synthesizing benzonitrile containing various substituent groups.

Copper-mediated cyanation of indoles and electron-rich arenes using DMF as a single surrogate

Zhang, Lianpeng,Lu, Ping,Wang, Yanguang

, p. 8322 - 8329 (2015/08/03)

The copper-mediated cyanation of indoles with DMF as a single surrogate has been realized. This approach could be applied for the cyanation of some electron-rich arenes and aryl aldehydes as well. Aryl aldehydes were demonstrated to be the key intermediates in the cascade process of cyanation of indoles and electron-rich arenes.

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