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Benzene, 2,4-dinitro-1-(2-propynyloxy)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

10242-20-3

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10242-20-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 10242-20-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,2,4 and 2 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 10242-20:
(7*1)+(6*0)+(5*2)+(4*4)+(3*2)+(2*2)+(1*0)=43
43 % 10 = 3
So 10242-20-3 is a valid CAS Registry Number.

10242-20-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4-dinitro-1-prop-2-ynoxybenzene

1.2 Other means of identification

Product number -
Other names 2,4-Dinitro-phenylpropargylether

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:10242-20-3 SDS

10242-20-3Relevant academic research and scientific papers

A regio- and diastereoselective platinum-catalyzed tandem [2+1]/[3+2] cycloaddition sequence

Achard, Thierry,Lepronier, Aymeric,Gimbert, Yves,Clavier, Herve,Giordano, Laurent,Tenaglia, Alphonse,Buono, Gerard

, p. 3552 - 3556 (2011)

Platinum complexes bearing phosphinous acids have efficiently promoted a tandem intermolecular sequence of [2+1]/[3+2] cycloaddition reactions. This process gave access to novel tricyclic systems and the cascade reactions were regio- and diastereoselective (see scheme; Cy=cyclohexyl). The [3+2] cycloaddition reaction was investigated further and two different alkyne partners were used. Copyright

Ruthenium-Catalyzed Tandem Carbene/Alkyne Metathesis/N-H Insertion: Synthesis of Benzofused Six-Membered Azaheterocycles

Padín, Damián,Saá, Carlos,Varela, Jesús A.

supporting information, (2020/03/30)

The Cp*RuCl-based catalyst enables expedient access to a variety of benzofused six-membered azaheterocycles from unprotected o-alkynylanilines and trimethylsilyldiazomethane through an unprecedent tandem carbene/alkyne metathesis/N-H insertion reaction. The transformation takes place under mild reaction conditions (room temperature, 15 min) and with excellent functional group tolerance. The synthetic utility of the final products and a mechanistic rationale are also discussed.

Design, synthesis and biological evaluation of novel 2-methylpyrimidine-4- ylamine derivatives as inhibitors of Escherichia coli pyruvate dehydrogenase complex E1

He, Junbo,Feng, Lingling,Li, Jing,Tao, Ruijuan,Wang, Fang,Liao, Xun,Sun, Qiushuang,Long, Qingwu,Ren, Yanliang,Wan, Jian,He, Hongwu

experimental part, p. 1665 - 1670 (2012/04/10)

As potential inhibitors of Escherichia coli pyruvate dehydrogenase complex E1 (PDHc E1), a series of novel 2-methylpyrimidine-4-ylamine derivatives were designed based on the structure of the active site of PDHc E1 and synthesized using 'click chemistry'.

A modular synthesis of alkynyl-phosphocholine headgroups for labeling sphingomyelin and phosphatidylcholine

Sandbhor, Mahendra S.,Key, Jessie A.,Strelkov, Ileana S.,Cairo, Christopher W.

supporting information; experimental part, p. 8669 - 8674 (2010/02/28)

(Figure Presented) A general route to phospho- and sphingolipids that incorporate an alkyne in the phosphocholine headgroup is described. The strategy preserves the ammonium functionality of the phosphocholine and can be easily modified to introduce desir

Novel exploration of the SNAr reaction

Raeppel, Stéphane,Raeppel, Franck,Suffert, Jean

, p. 794 - 796 (2007/10/03)

Propargylic, allylic and benzylic alcohols prove to be fairly successful as activated nucleophiles, under mild conditions for the SNAr reaction.

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