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4-(PHENYLTHIO)OCTANOPHENONE, with the molecular formula C20H20OS, is an organic compound characterized by a phenylthio group attached to the fourth carbon of an octanophenone chain. 4-(PHENYLTHIO)OCTANOPHENONE is known for its low solubility in water and is typically utilized in organic solvents for chemical reactions. Its properties and applications can vary depending on the manufacturer and the intended use, making it a versatile intermediate in the synthesis of pharmaceuticals and organic materials.

17792-67-5

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17792-67-5 Usage

Uses

Used in Pharmaceutical Industry:
4-(PHENYLTHIO)OCTANOPHENONE serves as a crucial intermediate in the synthesis of various pharmaceuticals. Its unique structure allows for the development of new drugs with potential therapeutic benefits.
Used in Organic Material Synthesis:
In the field of organic materials, 4-(PHENYLTHIO)OCTANOPHENONE is used as an intermediate for creating a range of products with specific properties. Its versatility in chemical reactions contributes to the development of innovative materials for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 17792-67-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,7,9 and 2 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 17792-67:
(7*1)+(6*7)+(5*7)+(4*9)+(3*2)+(2*6)+(1*7)=145
145 % 10 = 5
So 17792-67-5 is a valid CAS Registry Number.

17792-67-5SDS

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 1-phenyl-4-phenylsulfanyloctan-1-one

1.2 Other means of identification

Product number -
Other names 4-n-Octanoyldiphenylsulfid

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:17792-67-5 SDS

17792-67-5Downstream Products

17792-67-5Relevant academic research and scientific papers

Preparation method of alpha-oximido acetophenone derivative

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Paragraph 0018-0020, (2020/06/20)

The invention discloses a preparation method of an alpha-oximido acetophenone derivative. The method comprises the following steps: adding acetophenone derivatives, ethyl acetate and hydrochloric acidinto a reaction kettle; after stirring and complete dissolution, introducing hydrogen chloride gas, adding nitrite at the temperature of 0-50 DEG C, keeping the temperature for 1-10 hours after feeding is finished, then washing with water, adjusting the pH value to be neutral, distilling ethyl acetate, and adding cyclohexane for crystallization after distillation is finished so as to obtain the alpha-oximido acetophenone derivative. According to the preparation method of the alpha-oximido acetophenone derivative, recycling of the solvent ethyl acetate can be achieved, the yield can be obviously increased by 90% or above, and the purity of a target object reaches 98% or above; the reaction is green and safe, and the raw material cost is low.

Ketone oxime ester photoinitiator green synthetic method

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Paragraph 0031; 0032; 0033, (2016/11/14)

The present invention discloses a ketone oxime ester photoinitiator green synthetic method. According to the method, diphenyl sulfide as a raw material is condensed with caprylyl chloride under the effect of a zirconium catalyst, and then a ketone oxime ester photoinitiator can be obtained by oximation and esterification. The method does not relate to high temperature and high pressure reaction, and is mild in reaction conditions, and good in security. No aluminum chloride or zinc waste water is produced due to use of the zirconium catalyst during the synthesis process, produced byproducts can be recycled, no environmentally harmful solvent is used, and the ketone oxime ester photoinitiator green synthetic method is environmentally friendly, and therefore suitable for industrial production.

OXIME ESTER COMPOUND AND A PHOTOPOLYMERIZABLE COMPOSITION COMPRISING THE SAME

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Paragraph 0099-0101; 0105, (2016/10/27)

The present invention relates to an oxime ester-based compound and a photopolymerizable composition comprising the same. More particularly, the present invention relates to a photopolymerizable composition comprising a photopolymerizable compound and a ph

OXIME ESTER COMPOUND AND A PHOTOPOLYMERIZABLE COMPOSITION COMPRISING THE SAME

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Paragraph 0107-0109, (2016/11/02)

The present invention relates to an oxime ester-based compound and a photopolymerizable composition comprising the same. More particularly, the present invention relates to a photopolymerizable composition comprising a photopolymerizable compound and a ph

OXIME ESTER COMPOUND AND A PHOTOPOLYMERIZABLE COMPOSITION COMPRISING THE SAME

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Sheet 13/22, (2017/02/24)

Disclosed herein is an oxime ester compound and a photopolymerizable composition comprising the same, more specifically, a photopolymerizable composition comprising photopolymerizable compound and photoinitiator, wherein the photoinitiator comprises oxime

OXIME ESTER COMPOUND AND A PHOTOPOLYMERIZABLE COMPOSITION COMPRISING THE SAME

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Page/Page column 12, (2017/02/24)

Disclosed herein is an oxime ester compound and a photopolymerizable composition comprising the same, more specifically, a photopolymerizable composition comprising a photopolymerizable compound and a photoinitiator, wherein the photoinitiator comprises o

OXIME ESTER COMPOUND AND A PHOTOPOLYMERIZABLE COMPOSITION COMPRISING THE SAME

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Paragraph 0098-0100; 0104, (2016/10/10)

The present invention relates to an oxime ester-based compound and a photopolymerizable composition comprising the same and, more specifically, to a photopolymerizable composition comprising a photopolymerizable compound and a photopolymerization initiato

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