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612-43-1

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612-43-1 Usage

General Description

2-Nitrobenzeneacrylic acid methyl ester is a chemical compound with the molecular formula C10H9NO4. It is a nitro-substituted acrylic acid ester that is commonly used in the production of dyes, pigments, and pharmaceuticals. It is also known for its potential use as a corrosion inhibitor and as a monomer in the production of polymers. 2-Nitrobenzeneacrylic acid methyl ester is considered a hazardous material and should be handled with care due to its toxicity and potential for causing skin and eye irritation. Its chemical structure consists of a nitrobenzene ring attached to an acrylic acid chain with a methyl ester group, making it a versatile and potentially valuable compound in various industrial and chemical processes.

Check Digit Verification of cas no

The CAS Registry Mumber 612-43-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,1 and 2 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 612-43:
(5*6)+(4*1)+(3*2)+(2*4)+(1*3)=51
51 % 10 = 1
So 612-43-1 is a valid CAS Registry Number.
InChI:InChI=1/C10H9NO4/c1-15-10(12)7-6-8-4-2-3-5-9(8)11(13)14/h2-7H,1H3/b7-6+

612-43-1SDS

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 methyl (E)-3-(2-nitrophenyl)prop-2-enoate

1.2 Other means of identification

Product number -
Other names nitrobenzamide

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:612-43-1 SDS

612-43-1Relevant articles and documents

Preparation method of 3-(2-aminophenyl)-2-acrylate

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Paragraph 0018-0019, (2022/01/12)

The present invention relates to the field of pharmaceutical preparation technology, in particular a 3-(2-aminophenyl)-2-acrylate preparation method, comprising the following steps: 1) under the action of a base, o-nitrobenzaldehyde and malonate derivativ

Enantioselective Rauhut–Currier Reaction with β-Substituted Acrylamides Catalyzed by N-Heterocyclic Carbenes

Pitchumani, Venkatachalam,Breugst, Martin,Lupton, David W.

supporting information, p. 9413 - 9418 (2021/12/09)

β-Substituted acrylamides have low electrophilicity and are yet to be exploited in the enantioselective Rauhut–Currier reaction. By exploiting electron-withdrawing protection of the amide and moderate nucleophilicity N-heterocyclic carbenes, such substrates have been converted to enantioenriched quinolones. The reaction proceeds with complete diastereoselectivity, good yield, and modest enantioselectivity. Derivatizations are reported, as are computational studies, supporting decreased amide bond character with electron-withdrawing protection of the nitrogen.

Access to [2,1]benzothiazine s,s-dioxides from β-substituted o-nitrostyrenes and sulfur

Mac, Dinh Hung,Nguyen, Thanh Binh,Nguyen, Thi Mo,Cao, Hoang Anh,Cao, Thi Thuong Thuong,Koyama, Satoki

, p. 12058 - 12066 (2020/11/10)

[2,1]Benzothiazine S,S-dioxides 2 were synthesized by simply heating o-nitrostyrenes with elemental sulfur in 3- picoline with complete atom economy. This reaction was found to occur without any added catalyst and consist of a cascade of reduction of the

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