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2-Butanone, 4-(2-nitrophenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

58751-62-5

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58751-62-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 58751-62-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,7,5 and 1 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 58751-62:
(7*5)+(6*8)+(5*7)+(4*5)+(3*1)+(2*6)+(1*2)=155
155 % 10 = 5
So 58751-62-5 is a valid CAS Registry Number.

58751-62-5SDS

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 4-(2-nitrophenyl)butan-2-one

1.2 Other means of identification

Product number -
Other names 2-Butanone,4-(2-nitrophenyl)

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:58751-62-5 SDS

58751-62-5Relevant academic research and scientific papers

The Heck reaction of allylic alcohols catalysed by an N-heterocyclic carbene-Pd(ii) complex and toxicity of the ligand precursor for the marine benthic copepod: Amphiascoides atopus

Cárdenas, Jorge,Gómez, Samuel,García-Ríos, Eréndira,Gavi?o, Ruben,López-Torres, Adolfo,Morales-Serna, Francisco Neptalí,Morales-Serna, José Antonio,Puello-Cruz, Ana C.,Rios-Ruiz, Lucero

, p. 20278 - 20284 (2021/06/28)

The palladium-catalysed reaction of aryl halides and allylic alcohols is an attractive method for obtaining α,β-unsaturated aldehydes and ketones, which represent key intermediates in organic synthesis. In this context, a 1,2,3-triazol-5-ylidene (aNHC)-based palladium(ii) complex formed in situ has been found to be a selective catalyst for the syntheses of building blocks from the corresponding aryl halides and allylic alcohols, with yields ranging from 50% to 90%. The lack of toxic effects of the ligand precursor (1,2,3-triazolium salt) of the palladium(ii) complex for the harpacticoid copepod Amphiascoides atopus allowed us to contrast the efficiency of the catalytic system with the potential impact of the principal waste chemical in global aquatic ecosystems, which has not been previously addressed.

Dopamine D2 receptor selective agonist and application thereof

-

Paragraph 0193; 0195, (2020/12/29)

The invention relates to a dopamine D2 receptor selective agonist and application thereof. Specifically, the invention discloses an agonist with selectivity to DRD2 and discloses a potential application value of the agonist in disease treatment. The invention discloses an agonist with DRD2 selectivity for the first time, and the specific targeting DRD2 of the agonist can play a role in treating low dopamine related diseases such as Parkinson's disease, attention deficit hyperactivity disorder, pituitary adenoma, hyperprolactinemia, hyperactivity leg syndrome, negative schizophrenia and the like while side effects are reduced to the maximum extent.

The Heck reaction of allylic alcohols catalysed by an air-stable phosphinito complex of palladium(II)

Sauza, Alejandro,Morales-Serna, Jose Antonio,Garcia-Molina, Monica,Gavino, Ruben,Cardenas, Jorge

experimental part, p. 272 - 282 (2012/04/17)

The Heck coupling of aryl bromides with primary and secondary allylic alcohols, performed in the presence of an air-stable- phosphinito complex of palladium(II), produced the corresponding carbonyl compounds. Reactions with tertiary allylic alcohols under the same conditions generated the aromatic conjugated alcohols. Georg Thieme Verlag Stuttgart · New York.

Improving the atom efficiency of the wittig reaction by a "waste as catalyst/Co-catalyst" strategy

Cao, Jun-Jie,Zhou, Feng,Zhou, Jian

supporting information; experimental part, p. 4976 - 4980 (2010/09/08)

(Figure Presented) Waste not want not: Reported is a strategy to improve the atom economy of the Wittig reaction by using it in tandem reactions that directly employ the wastePh3PO as an in-situ-generated Lewis base catalyst/co-catalyst in the next step (see scheme).

Arenediazonium o-benzenedisulfonimides in Heck-type arylation of allylic alcohols

Barbero, Margherita,Cadamuro, Silvano,Dughera, Stefano

, p. 3443 - 3452 (2008/02/12)

Arenediazonium o-benzenedisulfonimides were reacted with primary and secondary allylic alcohols. The reactions, carried out in aqueous ethanol in the presence of palladium(II) acetate as precatalyst and sodium hydrogen carbonate as base, gave the arylation products with good overall conversion. In all cases, the major products were the β-arylated carbonyl derivatives. The o-benzene-disulfonimide was recovered in high yield from all the reactions, and it was recycled for the preparation of other salts. Georg Thieme Verlag Stuttgart.

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