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1-(2'-Chlorobiphenyl-3-yl)ethan-1-one, also known as 2'-chloro-3-biphenylcarboxaldehyde, and 3-(2-Chlorophenyl)acetophenone, also known as 3-Acetyl-2-chloroanisole, are aromatic ketones with a chlorine substituent. They are chemical compounds with the formulas C14H11ClO and C14H11ClO, respectively. The former is a yellow to light brown solid, while the latter is a white to off-white solid. Both are used as intermediates in organic synthesis and have applications in various industries.

675596-35-7

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675596-35-7 Usage

Uses

Used in Pharmaceutical Industry:
1-(2'-Chlorobiphenyl-3-yl)ethan-1-one, 3-(2-Chlorophenyl)acetophenone is used as an intermediate for the synthesis of various pharmaceuticals. Their unique chemical structures allow them to be key components in the development of new drugs and medications.
Used in Perfumery Industry:
3-(2-Chlorophenyl)acetophenone is used as a component in the production of perfumes. Its aromatic properties contribute to the creation of various fragrances and scents.
Used in Organic Synthesis:
Both 1-(2'-Chlorobiphenyl-3-yl)ethan-1-one and 3-(2-Chlorophenyl)acetophenone are used as intermediates in organic synthesis. Their versatility in chemical reactions makes them valuable for the production of a wide range of organic compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 675596-35-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,7,5,5,9 and 6 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 675596-35:
(8*6)+(7*7)+(6*5)+(5*5)+(4*9)+(3*6)+(2*3)+(1*5)=217
217 % 10 = 7
So 675596-35-7 is a valid CAS Registry Number.

675596-35-7Downstream Products

675596-35-7Relevant academic research and scientific papers

Pd-EDTA as an efficient catalyst for Suzuki-Miyaura reactions in water

Korolev, Dmitrii N.,Bumagin, Nikolay A.

, p. 5751 - 5754 (2007/10/03)

PdCl2-EDTA complex 1 is an efficient catalyst for the Suzuki-Miyaura reactions of aryl and heteroaryl halides with aryl(heteroaryl)boronic acids in water at 20-100°C. Aryl iodides and bromides undergo the cross-coupling with turnover numbers (T

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