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94-30-4

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94-30-4 Usage

Chemical Properties

Different sources of media describe the Chemical Properties of 94-30-4 differently. You can refer to the following data:
1. clear yellow liquid
2. Ethyl p-anisate has a sweet, fruity, anise-like taste and similar odor.

Occurrence

Reported found in feijoa fruit, rum, white wine, plum (fresh), starfruit and guava.

Preparation

By esterification of anisic acid with ethanol in the presence of an acid catalyst.

Taste threshold values

Taste characteristics at 30 ppm: anise, sweet, fruity, licorice, grape and cherry-like.

Safety Profile

Moderately toxic by ingestion. See also ESTERS. Combustible liquid. When heated to decomposition it emits acrid smoke and irritating fumes.

Check Digit Verification of cas no

The CAS Registry Mumber 94-30-4 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 9 and 4 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 94-30:
(4*9)+(3*4)+(2*3)+(1*0)=54
54 % 10 = 4
So 94-30-4 is a valid CAS Registry Number.
InChI:InChI=1/C10H12O3/c1-3-7-6-8(13-2)4-5-9(7)10(11)12/h4-6H,3H2,1-2H3,(H,11,12)/p-1

94-30-4 Well-known Company Product Price

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  • Alfa Aesar

  • (A14008)  Ethyl 4-methoxybenzoate, 98+%   

  • 94-30-4

  • 50g

  • 280.0CNY

  • Detail
  • Alfa Aesar

  • (A14008)  Ethyl 4-methoxybenzoate, 98+%   

  • 94-30-4

  • 250g

  • 1058.0CNY

  • Detail
  • Alfa Aesar

  • (A14008)  Ethyl 4-methoxybenzoate, 98+%   

  • 94-30-4

  • 1000g

  • 3623.0CNY

  • Detail

94-30-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethyl p-Anisate

1.2 Other means of identification

Product number -
Other names Benzoic acid, 4-methoxy-, ethyl ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Food additives -> Flavoring Agents
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:94-30-4 SDS

94-30-4Relevant articles and documents

Mechanistic insight into the synergistic Cu/Pd-catalyzed carbonylation of aryl iodides using alcohols and dioxygen as the carbonyl source

Li, Junxuan,Zhou, Jinlei,Wang, Yumei,Yu, Yue,Liu, Qiang,Yang, Tilong,Chen, Huoji,Cao, Hua

, p. 68 - 74 (2021/11/16)

Pd-catalyzed carbonylation, as an efficient synthetic approach to the installation of carbonyl groups in organic compounds, has been one of the most important research fields in the past decade. Although elegant reactions that allow highly selective carbonylations have been developed, straightforward routes with improved reaction activity and broader substrate scope remain long-term challenges for new practical applications. Here, we show a new type of synergistic Cu/Pd-catalyzed carbonylation reaction using alcohols and dioxgen as the carbonyl sources. A broad range of aryl iodides and alcohols are compatible with this protocol. The reaction is concise and practical due to the ready availability of the starting materials and the scalability of the reaction. In addition, the reaction affords lactones and lactams in an intermolecular fashion. Moreover, DFT calculations have been performed to study the detailed mechanisms. [Figure not available: see fulltext.]

Pleuromutilin derivative with 1, 3, 4-oxadiazole side chain and preparation and application thereof

-

Paragraph 0055-0056; 0070; 0090; 0092; 0095; 0103, (2021/07/24)

The invention belongs to the field of medicinal chemistry, and particularly relates to a pleuromutilin derivative with a 1, 3, 4-oxadiazole side chain and preparation and application thereof The pleuromutilin derivative with the 1, 3, 4-oxadiazole side chain is a compound shown in a formula 2 or a pharmaceutically acceptable salt thereof, and a solvent compound, an enantiomer, a diastereoisomer and a tautomer of the compound shown in the formula 2 or the pharmaceutically acceptable salt thereof or a mixture of the solvent compound, the enantiomer, the diastereoisomer and the tautomer in any proportion, including a racemic mixture. The pleuromutilin derivative has good antibacterial activity, is especially suitable for being used as a novel antibacterial agent for systemic system infection of animals or human beings, and has good water solubility.

Electro-Oxidative Selective Esterification of Methylarenes and Benzaldehydes

Yu, Congjun,?zkaya, Bünyamin,Patureau, Frederic W.

supporting information, p. 3682 - 3687 (2021/02/01)

A mild and green electro-oxidative protocol to construct aromatic esters from methylarenes and alcohols is herein reported. Importantly, the reaction is free of metals, chemical oxidants, bases, acids, and operates at room temperature. Moreover, the design of the electrolyte was found critical for the oxidation state and structure of the coupling products, a rarely documented effect. This electro-oxidative coupling process also displays exceptional tolerance of many fragile easily oxidized functional groups such as hydroxy, aldehyde, olefin, alkyne, as well as neighboring benzylic positions. The enantiomeric enrichment of some chiral alcohols is moreover preserved during this electro-oxidative coupling reaction, making it overall a promising synthetic tool.

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