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58609-73-7

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58609-73-7 Usage

Synthesis Reference(s)

The Journal of Organic Chemistry, 50, p. 5370, 1985 DOI: 10.1021/jo00225a072Synthetic Communications, 14, p. 1365, 1984 DOI: 10.1080/00397918408057677

Check Digit Verification of cas no

The CAS Registry Mumber 58609-73-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,6,0 and 9 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 58609-73:
(7*5)+(6*8)+(5*6)+(4*0)+(3*9)+(2*7)+(1*3)=157
157 % 10 = 7
So 58609-73-7 is a valid CAS Registry Number.
InChI:InChI=1/C13H17N/c1-10(2)8-12-4-6-13(7-5-12)11(3)9-14/h4-7,10-11H,8H2,1-3H3

58609-73-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (±)-2-(4'-isobutylphenyl)propionitrile

1.2 Other means of identification

Product number -
Other names (+-)-2-(4'-isobutylphenyl)propionitrile

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:58609-73-7 SDS

58609-73-7Relevant articles and documents

Electrochemical Benzylic C-H Functionalization with Isocyanides

Grimaud, Laurence,Guillot, Régis,Tang, Shanyu,Vincent, Guillaume,Vitale, Maxime R.

supporting information, p. 2125 - 2130 (2022/04/07)

We report the challenging direct carbamoylation or cyanation of benzylic C(sp3)-H bonds with an isocyanide via an electrochemical process giving rise to structures that are encountered in several biologically relevant compounds and drugs. This transformation proceeds under mild conditions without the need for any external oxidant and avoids the necessity to start from a prefunctionalized benzylic substrate or the deployment of the cation pool method. The anodic oxidation of the benzylic position and the subsequent addition of the isocyanide lead to the formation of a C-C bond and to a nitrilium cation that hydrolyzes to yield α-Aryl acetamide derivatives, whereas the elimination of a t-butyl cation delivers α-Aryl acetonitrile derivatives.

CONTINUOUS FLOW SYNTHESIS OF IBUPROFEN

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Paragraph 0034-0035; 0411, (2021/04/23)

This disclosure generally relates to methods of making ibuprofen, naproxen, and derivatives thereof. This disclosure also generally relates to compounds made by the disclosed methods. This abstract is intended as a scanning tool for purposes of searching in the particular art and is not intended to be limiting of the present invention.

Application of novel dimethyl carbonate methylation catalyst in preparation α- methyl phenylacetic acid

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Paragraph 0059-0061, (2020/03/17)

The invention relates to the field, of medicine synthesis, and concretely relates to a novel dimethyl carbonate methylation catalyst α - in preparation IV methylbenzene acetic acid. as starting material I for preparing a target product, methylbenzeneacetic acid, by a methylation, decarboxylation and hydrolysis reaction, under the action of a catalyst by using a catalyst as a representative low-cost catalyst, in the form of a quaternary amine salt, and a catalyst prepared by using the catalyst as a representative low-cost catalyst, such as potassium α - potassium bromide acetate, as a catalyst, and a catalyst used in the, hydrolysis reaction of the quaternary, amine salt. IV. 98%. The preparation method comprises the following steps: preparing a target product from the quaternary ammonium. salt solution.

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