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1-Butanone, 4-ethoxy-1,4-diphenyl-, also known as 4-Ethoxy-1,4-diphenylbutan-1-one, is an organic compound with the chemical formula C18H20O2. It is a colorless liquid with a molecular weight of 272.35 g/mol. 1-Butanone, 4-ethoxy-1,4-diphenyl- is characterized by the presence of a butanone group (a four-carbon ketone) with two phenyl groups attached to the first and fourth carbon atoms, and an ethoxy group (an ethyl ether) attached to the fourth carbon as well. It is used in various chemical reactions and as an intermediate in the synthesis of other organic compounds. Due to its chemical structure, it may have potential applications in the pharmaceutical and chemical industries. However, it is important to handle 1-Butanone, 4-ethoxy-1,4-diphenyl- with care, as it may have hazardous properties and should be used in accordance with proper safety guidelines.

5604-61-5

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5604-61-5 Usage

Physical form

Colorless liquid

Odor

Sweet, fruity

Solubility

Soluble in water

Usage

Solvent in industrial and laboratory applications, production of fragrances, flavors, and other chemical products

Potential applications

Pharmaceutical and cosmetic industries

Precaution

May pose health hazards if not used properly

Check Digit Verification of cas no

The CAS Registry Mumber 5604-61-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,0 and 4 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5604-61:
(6*5)+(5*6)+(4*0)+(3*4)+(2*6)+(1*1)=85
85 % 10 = 5
So 5604-61-5 is a valid CAS Registry Number.

5604-61-5Downstream Products

5604-61-5Relevant academic research and scientific papers

A metal-free transformation of alkynes to carbonyls directed by remote OH group

Chen, Dao-Qian,Guo, Chun-Huan,Zhang, Heng-Rui,Jin, Dong-Po,Li, Xue-Song,Gao, Pin,Wu, Xin-Xing,Liu, Xue-Yuan,Liang, Yong-Min

supporting information, p. 4176 - 4180 (2016/08/02)

A remote OH group-directed metal-free transformation of alkynes to carbonyl compounds has been developed. Using only HOAc and EtOH solvent, this reaction elegantly converts alkynes into valuable ketones by remote hydroxyl group activation. Through comparison and isotope labeling experiments, it was confirmed that the process operates via a hydration reaction involving an acetic acid molecule, instead of a water molecule.

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