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"Acetamide, N-[4-(ethenyloxy)phenyl]-" is a chemical compound with the molecular formula C11H11NO2. It is an organic compound that belongs to the class of acetamides, which are derivatives of acetic acid. This specific acetamide features a phenyl group (a benzene ring) with a 4-(ethenyloxy) substituent, where "ethenyloxy" refers to a vinyloxy group, which is an ethylene oxide group (-CH2CH2O-). The compound is characterized by its amide linkage, where the nitrogen atom is bonded to the carbonyl carbon of the acetamide group. It is used in various applications, including as an intermediate in the synthesis of pharmaceuticals and other organic compounds. Due to its specific structure, it may exhibit unique chemical properties and reactivity patterns, making it a valuable component in the development of new materials and drugs.

830-04-6

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830-04-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 830-04-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,3 and 0 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 830-04:
(5*8)+(4*3)+(3*0)+(2*0)+(1*4)=56
56 % 10 = 6
So 830-04-6 is a valid CAS Registry Number.

830-04-6SDS

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 N-(4-ethenoxyphenyl)acetamide

1.2 Other means of identification

Product number -
Other names 4-Acetaminophenyl-vinylether

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:830-04-6 SDS

830-04-6Relevant academic research and scientific papers

Solid-Phase synthesis of aryl vinyl ethers based on polystyrenesupported aβ-phenylselenoethanol

Zhang, Jia-Li,Sheng, Shou-Ri,Liub, Xue,Lin, Shu-Ying

experimental part, p. 287 - 289 (2010/02/28)

A novel facile solid-phase organic synthesis of aryl vinyl ethers by reaction of polystyrene-supported β-phenylselenoethanol with phenols under Mitsunobu conditions and subsequent oxidation-elimination with 30% hydrogen peroxide has been developed. The ad

β-Phenylselenoethanol, an efficient reagent for the one-pot synthesis of aryl vinyl ethers

Fu, Gui-Yun,Yu, La-Mei,Mao, Xue-Chun,Wu, Dan

experimental part, p. 595 - 597 (2009/10/15)

β-Phenylselenoethanol was treated with phenols under Mitsunobu conditions and subsequent oxidation-elimination with 30% hydrogen peroxide furnished aryl vinyl ethers with good yields (85-90%) in a one-pot, two-step transformation.

Polymer-supported β-bromoethyl selenide: An efficient reagent for the synthesis of aryl vinyl ethers

Sheng, Shou-Ri,Liu, Xiao-Ling,Wang, Xing-Cong,Xin, Qin,Song, Cai-Sheng

, p. 2833 - 2836 (2007/10/03)

A simple and efficient procedure for the solid-phase synthesis of aryl vinyl ethers using polymer-supported β-bromoethyl selenide with traceless linker strategy is described.

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