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1-(1-methylethoxy)-4-[(E)-2-nitroethenyl]benzene is an organic compound characterized by a benzene ring with a methyl ethoxy group at the 1-position and a nitroethenyl group at the 4-position. The nitroethenyl group is in the E configuration, indicating that the nitro group and the ethoxy group are on opposite sides of the double bond. 1-(1-methylethoxy)-4-[(E)-2-nitroethenyl]benzene is a derivative of benzene, with the methyl ethoxy group providing a hydroxyl group and an ethyl group, while the nitroethenyl group introduces a nitro group and a double bond. The compound may have potential applications in the synthesis of pharmaceuticals, dyes, or other organic compounds due to its unique structure and functional groups.

6946-32-3

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6946-32-3 Usage

Chemical structure

Nitroalkene compound

Explanation

Nitroalkene compounds are organic molecules that contain a nitro group (-NO2) and an alkene group (a carbon-carbon double bond) in their structure.

Explanation

The benzene ring is a six-carbon ring with alternating single and double bonds. In 1-(1-methylethoxy)-4-[(E)-2-nitroethenyl]benzene, it is substituted by a 1-(1-methylethoxy) group and a 2-nitroethenyl group.

Explanation

The 1-(1-methylethoxy) group is an ethoxy group (-OCH2CH3) with a methyl group (-CH3) attached to the carbon atom next to the oxygen atom.

Explanation

The 2-nitroethenyl group is a vinyl group (-CH=CH2) with a nitro group (-NO2) attached to the second carbon atom. The E configuration indicates that the nitro group and the hydrogen atom on the double bond are on the same side of the molecule.

Explanation

1-(1-methylethoxy)-4-[(E)-2-nitroethenyl]benzene is used as an intermediate in the synthesis of various organic compounds, including pharmaceuticals and agrochemicals.

Explanation

Due to its chemical properties, 1-(1-methylethoxy)-4-[(E)-2-nitroethenyl]benzene can cause skin and eye irritation upon contact. Inhalation of its vapors or dust can also lead to respiratory problems.

Explanation

It is essential to follow proper safety protocols when handling this chemical compound to minimize the risk of exposure and potential health hazards.

Benzene ring

Substituted by two functional groups

1-(1-methylethoxy) group

A methyl group attached to an ethoxy group

2-nitroethenyl group

A nitro group attached to a vinyl group in E configuration

Applications

Organic synthesis, pharmaceuticals, and agrochemicals

Health hazards

Skin and eye irritation, respiratory issues

Safety precautions

Handle with care

Check Digit Verification of cas no

The CAS Registry Mumber 6946-32-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,4 and 6 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6946-32:
(6*6)+(5*9)+(4*4)+(3*6)+(2*3)+(1*2)=123
123 % 10 = 3
So 6946-32-3 is a valid CAS Registry Number.

6946-32-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[(E)-2-nitroethenyl]-4-propan-2-yloxybenzene

1.2 Other means of identification

Product number -
Other names 1-isopropoxy-3-methyl-2,5-dihydro-1H-phosphole 1-oxide

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:6946-32-3 SDS

6946-32-3Relevant academic research and scientific papers

Total synthesis of (±)-armepavines and (±)-nuciferines from (2-nitroethenyl)benzene derivatives

Chang, Chia-Fu,Huang, Chu-Yun,Huang, Yu-Chao,Lin, Kuan-Yu,Lee, Yean-Jang,Wang, Chau-Jong

experimental part, p. 3452 - 3466 (2011/02/22)

A concise route to armepavine 1 and nuciferine 2 and 3, which can be isolated from the leaves of Nelumbo nucifera (Nymphaceae), has been achieved in which the longest linear sequence is only six steps from commercially available benzaldehyde in 28%, 21%, and 20% overall yield, respectively. The key transformations in the synthesis are the radical cyclization of aryl bromide with Bu3SnH and the Pictet-Spengler reaction of N-substituted amine with aldehyde. Copyright Taylor & Francis Group, LLC.

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