Welcome to LookChem.com Sign In|Join Free
  • or
4-Chloro-1-phenyl-1-butene is an organic compound with the molecular formula C10H11Cl. It is a colorless liquid with a distinct aromatic odor. This chemical is a derivative of 1-butene, featuring a phenyl group (C6H5) attached to the first carbon and a chlorine atom (Cl) attached to the fourth carbon. The presence of the phenyl group imparts some aromatic characteristics, while the chlorine atom introduces reactivity and potential for further chemical reactions. 4-Chloro-1-phenyl-1-butene is used in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals due to its unique structure and reactivity. It is also known for its potential applications in the field of materials science, particularly in the development of polymers and other advanced materials.

1794-47-4

Post Buying Request

1794-47-4 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

1794-47-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1794-47-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,9 and 4 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1794-47:
(6*1)+(5*7)+(4*9)+(3*4)+(2*4)+(1*7)=104
104 % 10 = 4
So 1794-47-4 is a valid CAS Registry Number.

1794-47-4Relevant academic research and scientific papers

Mechanism of the Reduction of Ketones by Trialkylsilane. Hydride Transfer, SET-Hydrogen Atom Abstraction, or Free Radical Addition

Yang, D.,Tanner, D. D.

, p. 2267 - 2270 (1986)

The mechanism for the fluoride ion catalyzed reduction of ketones with phenyldimethylsilane was investigated.With reactive substrates (i.e., α,α,α-trifluoroacetophenone) the silane can act as a reducing agent to give, upon hydrolysis, moderate yields of the corresponding alcohol.The pentavalent anion formed from the silane and fluoride anion is, as had been previously reported, an excellent hydride reducing agent and even with moderate acceptors (i.e., α-fluoroacetophenone and cyclopropyl phenyl ketone) the anion acts as a SET reagent to give minor amounts of radical derived reduction products.

Light-Promoted Copper-Catalyzed Enantioselective Alkylation of Azoles

Li, Chen,Chen, Bin,Ma, Xiaodong,Mo, Xueling,Zhang, Guozhu

supporting information, p. 2130 - 2134 (2020/11/30)

A catalytic asymmetric alkylation of azoles with secondary 1-arylalkyl bromides through direct C?H functionalization is reported. Under blue-light photoexcitation, a copper(I)/carbazole-based bisoxazoline (CbzBox) catalytic system exhibits good reactivity and high stereoselectivity, thus offering an efficient strategy for the construction of chiral alkyl azoles. These reactions proceed at low temperature and are compatible with a wide range of azoles.

Preparation method for p-phenylbutoxybenzoic acid

-

Paragraph 0070-0071; 0078-0079, (2019/11/04)

The invention provides a preparation method for p-phenylbutoxybenzoic acid, belonging to the field of organic synthesis. According to the invention, palladium-based catalytic coupling is adopted, andthe Grignard reaction and the Friedel-Craft reaction are avoided, thereby avoiding the production of blue-green copper ion wastewater and generation of a large amount of acidic wastewater due to usageof aluminum trichloride; the preparation method of the invention is friendly to environment, simple in synthesis route and high in the yield of each step; and halogeno-benzene is used for replacing more expensive phenylmagnesium bromide and used as a starting material, so the preparation cost of p-phenylbutoxybenzoic acid is lowered. The p-phenylbutoxybenzoic acid obtained in the invention has good crystal form, high purity and good solubility. The data of embodiments of the invention show that the total yield of p-phenylbutoxybenzoic acid prepared in the invention is 60% or above, and the HPLC purity of p-phenylbutoxybenzoic acid is 99.9% or above.

Potassium Chlorochromate on a Solid Support: A Convenient and Mild Reagent for the Oxidation of Alcohols

Carlsen, Per H. J.,Husbyn, Mette,Braenden, Jon E,,Eliason, Robert

, p. 485 - 488 (2007/10/02)

The oxidation of primary and secondary alcohols by potassium chlorochromate supported on alumina or silica gel is reported.The results indicate that the yields in some cases depend on the support medium.Benzylic and secondary alcohols are oxidized in the best yields.The effect of solvent on the reaction is discussed and the conclusion is drawn that the best yields are obtained in non-polar solvents.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 1794-47-4