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2,5-Bis(trifluoromethyl)iodobenzene, with the molecular formula C8H3F6I, is a solid, crystalline chemical compound. It is renowned for its high reactivity, which allows it to engage in a variety of substitution and coupling reactions. 2,5-BIS(TRIFLUOROMETHYL)IODOBENZENE is particularly noted for its utility in organic synthesis and as a reagent in chemical reactions, often serving to introduce the trifluoromethyl group into organic molecules. Its presence of trifluoromethyl and iodine functional groups renders it a highly valuable asset in synthetic chemistry, especially for the construction of complex molecules.

328-92-7

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328-92-7 Usage

Uses

Used in Organic Synthesis:
2,5-BIS(TRIFLUOROMETHYL)IODOBENZENE is used as a reagent for introducing the trifluoromethyl group into organic molecules, which is crucial for creating a range of complex compounds with potential applications in various fields.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 2,5-BIS(TRIFLUOROMETHYL)IODOBENZENE is used as a building block for the development of new compounds with potential biological activities. Its unique properties make it a valuable component in the synthesis of drugs with novel therapeutic effects.
Used in Agrochemical Research:
Similarly, in agrochemical research, 2,5-BIS(TRIFLUOROMETHYL)IODOBENZENE is employed as a starting material for creating new compounds that may exhibit beneficial effects in agricultural applications, such as pest control and crop protection.
Used in Chemical Reactions:
2,5-BIS(TRIFLUOROMETHYL)IODOBENZENE is utilized in various substitution and coupling reactions due to its high reactivity, making it an essential tool in the synthesis of a wide array of chemical products.

Check Digit Verification of cas no

The CAS Registry Mumber 328-92-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,2 and 8 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 328-92:
(5*3)+(4*2)+(3*8)+(2*9)+(1*2)=67
67 % 10 = 7
So 328-92-7 is a valid CAS Registry Number.

328-92-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Iodo-1,4-bis(trifluoromethyl)benzene

1.2 Other means of identification

Product number -
Other names PC9312

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:328-92-7 SDS

328-92-7Relevant academic research and scientific papers

Single C?F Bond Cleavage of Trifluoromethylarenes with an ortho-Silyl Group

Yoshida, Suguru,Shimomori, Ken,Kim, Youngchan,Hosoya, Takamitsu

supporting information, p. 10406 - 10409 (2016/08/24)

The transformation of a single C?F bond of trifluoromethylarenes bearing a hydrosilyl group at the ortho position was achieved. The activation of the hydrosilyl group with a trityl cation in the presence of nucleophiles allowed for selective C?F bond func

TRICYCLIC COMPOUNDS AS mPGES-1 INHIBITORS

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Page/Page column 44, (2012/09/10)

The present invention relates to tricyclic compounds of formula (I) or pharmaceutically acceptable salt thereof as mPGES-1 inhibitors. These compounds are inhibitors of the microsomal prostaglandin E synthase-1 (mPGES-1) enzyme and are therefore useful in the treatment of pain and/or inflammation from a variety of diseases or conditions, such as asthama, osteoarthritis, rheumatoid arthritis, acute or chronic pain and neurodegenerative diseases. (I)

A scaleable synthesis of dutasteride: A selective 5α-reductase inhibitor

Satyanarayana, Komati,Srinivas, Katkam,Himabindu, Vurimidi,Reddy, Ghanta Mahesh

, p. 842 - 845 (2012/12/30)

An improved and scaleable process for Dutasteride (1), a synthetic 4-azasteroid derivative essentially used for the treatment of prostate diseases, is described

Process for the preparation of 17beta-N-[2,5-bis(trifluoromethyl)phenyl] carbamoyl-4-aza-5-alpha-androst-1-en-3-one

-

Page/Page column 3; 4, (2008/06/13)

The present invention relates to a process for the preparation of Dutasteride, which is chemically known as 17β-N-[2,5-bis (trifluoromethyl) phenyl] carbamoyl-4-aza-5-α-androst-1-en-3-one and can be represented by Formula (I).

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