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113352-66-2

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113352-66-2 Usage

Description

1-(4-Methoxy-2-nitrophenyl)propan-2-one is a nitroaromatic chemical compound characterized by the molecular formula C10H11NO4. It is a yellow solid with a molecular weight of 221.199 g/mol, known for its aromatic and aliphatic properties. 1-(4-Methoxy-2-nitrophenyl)propan-2-one is commonly used as an intermediate in the synthesis of various pharmaceuticals and organic compounds, and is also utilized in the production of dyes, pigments, and other industrial applications due to its unique chemical properties and reactivity.

Uses

Used in Pharmaceutical Industry:
1-(4-Methoxy-2-nitrophenyl)propan-2-one is used as a chemical intermediate for the synthesis of various pharmaceuticals, contributing to the development of new drugs and medications.
Used in Organic Chemistry:
1-(4-Methoxy-2-nitrophenyl)propan-2-one is used as a reactant in various organic chemistry reactions, facilitating the formation of different organic compounds and aiding in the advancement of chemical research.
Used in Dye and Pigment Production:
1-(4-Methoxy-2-nitrophenyl)propan-2-one is used in the production of dyes and pigments, providing unique color properties and enhancing the quality of these products for various applications.
Used in Other Industrial Applications:
Due to its reactivity and chemical properties, 1-(4-Methoxy-2-nitrophenyl)propan-2-one is also utilized in other industrial applications, contributing to the development and improvement of various products and processes.

Check Digit Verification of cas no

The CAS Registry Mumber 113352-66-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,3,5 and 2 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 113352-66:
(8*1)+(7*1)+(6*3)+(5*3)+(4*5)+(3*2)+(2*6)+(1*6)=92
92 % 10 = 2
So 113352-66-2 is a valid CAS Registry Number.

113352-66-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-methoxy-2-nitrophenyl)propan-2-one

1.2 Other means of identification

Product number -
Other names 2-nitro-4-methoxyphenylacetone

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:113352-66-2 SDS

113352-66-2Relevant articles and documents

A practical synthesis of α-aryl methyl ketones via a transition-metal-free Meerwein arylation

Molinaro, Carmela,Mowat, Jeffrey,Gosselin, Francis,O'Shea, Paul D.,Marcoux, Jean-Francois,Angelaud, Remy,Davies, Ian W.

, p. 1856 - 1858 (2007)

We report herein a simple, scalable, transition-metal-free approach to the synthesis of α-aryl methyl ketones from diazonium tetrafluoroborate salts under mild conditions. This methodology uses easily accessible and nontoxic starting material and was applied to the multi-kilogram-scale preparation of 1-(3-bromo-4-methylphenyl)propan-2-one.

C-C Activation by Retro-Aldol Reaction of Two β-Hydroxy Carbonyl Compounds: Synergy with Pd-Catalyzed Cross-Coupling to Access Mono-α-arylated Ketones and Esters

Zhang, Song-Lin,Yu, Ze-Long

, p. 57 - 65 (2016/01/15)

A retro-aldol reaction of two β-hydroxy compounds in synergy with Pd-catalyzed cross-coupling of aryl halides is reported herein, which produces selectively mono-α-arylated ketones and esters in good yields. This reaction is compatible with a broad range of aryl iodides, bromides, chlorides, and triflates and can tolerate an array of functional groups on the aromatic ring. Ready scale-up of this reaction to gram level is applicable without an appreciable decrease in the reaction yield. Furthermore, concise syntheses of biologically active isocoumarin and indole derivatives have been achieved to greatly demonstrate the synthetic value of this retro-aldol reaction. Finally, the reaction mechanism has been discussed on the basis of experimental observations and DFT computational results. A regulated six-membered-ring transition structure has been located for the key retro-aldol C-C cleavage, which constitutes the rate-determining step of a full catalytic cycle. The concept of C-C activation by retro-aldol reaction may also find applications in other fundamental reactions.

OPHTHALMIC COMPOSITIONS FOR TREATING OCULAR HYPERTENSION

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Page 34-35, (2010/11/30)

This invention relates to the use of potent potassium channel blockers or a formulation thereof in the treatment of glaucoma and other conditions which leads to elevated intraoccular pressure in the eye of a patient. This invention also relates to the use

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