(2-Chloro-5-iodophenyl)(4-fluorophenyl)methanone

  • CAS:915095-86-2
  • purity:99%
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Quality products?make an important contribution to long-term revenue and profitability. China cas 915095-86-2 factory wholesale (2-Chloro-5-iodophenyl)(4-fluorophenyl)methanone at affordable price

1.What is the (2-Chloro-5-iodophenyl)(4-fluorophenyl)methanone ?

(2-Chloro-5-iodophenyl)(4-fluorophenyl)methanone is a reagent in the synthesis of Empagliflozin (E521510); an inhibitor of SGLT-2.

2-chloro-5-iodobenzoylchloride
281652-58-2

2-chloro-5-iodobenzoylchloride

fluorobenzene
462-06-6

fluorobenzene

(2-chloro-5-iodophenyl)(4-fluorophenyl)methanone
915095-86-2

(2-chloro-5-iodophenyl)(4-fluorophenyl)methanone

Conditions
Conditions Yield
With aluminum (III) chloride; In dichloromethane; at -5 ℃; for 6h;
93.4%
2-chloro-5-iodobenzoylchloride; fluorobenzene; With aluminum (III) chloride; at 0 - 75 ℃; for 1.5h;
With water; at 0 - 25 ℃;
With aluminum (III) chloride; at 0 - 25 ℃; for 1h; regioselective reaction;
121 g
With aluminum (III) chloride; at 25 ℃; Inert atmosphere;
105 g
With aluminum (III) chloride; In dichloromethane; at 20 ℃; for 3h; Cooling with ice;
42.1 g
fluorobenzene
462-06-6

fluorobenzene

2-chloro-5-iodobenzoic acid
19094-56-5

2-chloro-5-iodobenzoic acid

(2-chloro-5-iodophenyl)(4-fluorophenyl)methanone
915095-86-2

(2-chloro-5-iodophenyl)(4-fluorophenyl)methanone

Conditions
Conditions Yield
With oxalyl dichloride; N,N-dimethyl-formamide; at 25 - 30 ℃; for 5h;
94%
fluorobenzene; 2-chloro-5-iodobenzoic acid; With oxalyl dichloride; In N,N-dimethyl-formamide; at 25 - 30 ℃; for 5h;
With aluminum (III) chloride; water; at 20 - 30 ℃; for 6h;
94%
With aluminum (III) chloride; oxalyl dichloride; In N,N-dimethyl-formamide; at 25 - 45 ℃; Industry scale;
94%
2-chloro-5-iodobenzoic acid; With oxalyl chloride; In dichloromethane; N,N-dimethyl-formamide; at 20 ℃; for 4h;
fluorobenzene; With aluminum (III) chloride; In dichloromethane; N,N-dimethyl-formamide; at 0 - 20 ℃; for 3h;
92%
2-chloro-5-iodobenzoic acid; With oxalyl dichloride; N,N-dimethyl-formamide; In dichloromethane; for 3h;
fluorobenzene; With aluminum (III) chloride; In dichloromethane; at 0 - 5 ℃; for 1h;
78.6%
2-chloro-5-iodobenzoic acid; With thionyl chloride; N,N-dimethyl-formamide; In dichloromethane; at 39 - 42 ℃;
fluorobenzene; With aluminum (III) chloride; Reflux;
310 g

2.What is the CAS number for (2-Chloro-5-iodophenyl)(4-fluorophenyl)methanone ?

The CAS number of (2-Chloro-5-iodophenyl)(4-fluorophenyl)methanone is 915095-86-2.

More information of (2-Chloro-5-iodophenyl)(4-fluorophenyl)methanone 915095-86-2 are:

CAS?Number

915095-86-2

Density

1.752

Boiling Point

415℃

Flash Point

205℃

HS CODE

29142990

PSA

17.07000

LogP

4.31470

3.What are another words for (2-Chloro-5-iodophenyl)(4-fluorophenyl)methanone ?

Synonyms?for?(2-Chloro-5-iodophenyl)(4-fluorophenyl)methanone 915095-86-2:Empagliflozin intermediate;(2-Chloro-5-iodophenyl)(4-fluorophenyl)methanone;

4.What is the molecular formula of (2-Chloro-5-iodophenyl)(4-fluorophenyl)methanone?

The chemical formula of ?(2-Chloro-5-iodophenyl)(4-fluorophenyl)methanone is?C13H7ClFIO which containing 13 Carbon atoms,7 Hydrogen atoms,1 Chlorine atoms,1 Fluorine atoms,1 Iodine atoms and 1 Oxygen atoms,and the molecular weight of??(2-Chloro-5-iodophenyl)(4-fluorophenyl)methanone?is 360.554.

5.What is (2-Chloro-5-iodophenyl)(4-fluorophenyl)methanone (915095-86-2) used for?

(2-Chloro-5-iodophenyl)(4-fluorophenyl)methanone is an organic compound that serves as a key intermediate in the synthesis of Empagliflozin (E521510), a potent inhibitor of the SGLT-2 enzyme. (2-Chloro-5-iodophenyl)(4-fluorophenyl)methanone is characterized by its unique structure, featuring a chloro and iodophenyl group connected to a fluorophenyl group through a methanone bridge. Its chemical properties make it a valuable reagent in pharmaceutical chemistry for the development of novel therapeutic agents.

Relevant articles related to (2-Chloro-5-iodophenyl)(4-fluorophenyl)methanone:

Article

Source

Dicyclic derivative of glucoside as well as preparation method and application of dicyclic derivative

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Paragraph 0196; 0197; 0198, (2018/07/30)

Preparation method of SGLT2 inhibitor intermediate

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Paragraph 0038-0039, (2017/08/30)

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