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2-Chloroethyl furan-2-carboxylate is an organic compound with the chemical formula C7H7ClO3. It is a derivative of furan-2-carboxylic acid, featuring a chloroethyl group attached to the furan ring. 2-chloroethyl furan-2-carboxylate is characterized by its potential reactivity due to the presence of the chloroethyl moiety, which can participate in various chemical reactions, such as nucleophilic substitutions. It is synthesized for use in the production of pharmaceuticals and other chemical compounds, where its unique structure can be leveraged for specific reactivity patterns. The compound is typically handled with care due to its potential toxicity and reactivity, and it is an example of the broad range of chemical structures that can be found in organic chemistry.

936-75-4

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936-75-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 936-75-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,3 and 6 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 936-75:
(5*9)+(4*3)+(3*6)+(2*7)+(1*5)=94
94 % 10 = 4
So 936-75-4 is a valid CAS Registry Number.

936-75-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-chloroethyl furan-2-carboxylate

1.2 Other means of identification

Product number -
Other names -

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 -
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More Details:936-75-4 SDS

936-75-4Downstream Products

936-75-4Relevant academic research and scientific papers

Method for generating ester through reaction of acyl chloride and 1,2-dichloroethane

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Paragraph 0023; 0025; 0065; 0066; 0067, (2017/08/30)

The invention discloses a method for generating ester through reaction of acyl chloride and 1,2-dichloroethane. The method comprises the following steps: taking acyl chloride, 1,2-dichloroethane and carbonate as reaction substrates, and taking 4-dimethyla

An Effective Method for the Construction of Esters Using Cs2CO3 as Oxygen Source

Ren, Lanhui,Wang, Lianyue,Lv, Ying,Li, Guosong,Gao, Shuang

supporting information, p. 5172 - 5175 (2015/11/24)

An effective method for the construction of esters from acyl chloride and halohydrocarbon using Cs2CO3 as an oxygen source was achieved for the first time. The methodology has a wide scope of substrates and can be scaled up. The study of a preliminary reaction mechanism demonstrated that the O in the products comes from Cs2CO3 and this esterification proceeds through a free radical reaction. It was also found that CO2 can also be used in this esterification reaction as an oxygen source.

Transition-metal-free aerobic oxidative cleavage of C-C bonds in α-hydroxy ketones and mechanistic insight to the reaction pathway

Liu, Hui,Dong, Chao,Zhang, Zeguang,Wu, Peiyu,Jiang, Xuefeng

supporting information, p. 12570 - 12574 (2013/02/22)

Clear cut: For the title reaction, O2, the ideal oxidant, was used as the only oxidizing reagent. The dimer intermediate (see scheme) and isotopic labeling control experiments with 18O2 partially disclosed the reaction mec

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