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(R)-2-((4-(TRIFLUOROMETHYL)PHENOXY)METHYL)OXIRANE, commonly known as fomesafen, is a selective herbicide belonging to the diphenyl ether chemical class. It is characterized by its ability to inhibit the enzyme protoporphyrinogen oxidase, which plays a crucial role in chlorophyll biosynthesis in plants. This herbicide is specifically designed to target and control a broad spectrum of broadleaf weeds in various agricultural crops.

851528-84-2

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851528-84-2 Usage

Uses

Used in Agriculture:
Fomesafen is used as a herbicide for controlling a wide range of broadleaf weeds in crops such as soybeans, peanuts, cotton, and sunflowers. Its application can be pre-emergence, post-emergence, or pre-plant incorporated, providing effective and long-lasting weed control. This helps to improve crop yield and quality by reducing competition from weeds.
However, it is essential to use fomesafen with caution due to its potential toxicity to aquatic organisms and the possibility of long-term environmental impacts if not managed properly. Proper application techniques and adherence to guidelines can help minimize these risks and ensure the sustainable use of this herbicide in agriculture.

Check Digit Verification of cas no

The CAS Registry Mumber 851528-84-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,1,5,2 and 8 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 851528-84:
(8*8)+(7*5)+(6*1)+(5*5)+(4*2)+(3*8)+(2*8)+(1*4)=182
182 % 10 = 2
So 851528-84-2 is a valid CAS Registry Number.

851528-84-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (2R)-2-[[4-(trifluoromethyl)phenoxy]methyl]oxirane

1.2 Other means of identification

Product number -
Other names Oxirane,2-[[4-(trifluoromethyl)phenoxy]methyl]-,(2R)

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:851528-84-2 SDS

851528-84-2Relevant articles and documents

Synthesis and biological evaluation of 1-(2-hydroxy-3-phenyloxypropyl) piperazine derivatives as T-type calcium channel blockers

Park, Jung-Eun,Ji, Wan Keun,Jang, Jae Wan,Pae, Ae Nim,Choi, Keehyun,Choi, Ki Hang,Kang, Jahyo,Roh, Eun Joo

supporting information, p. 1887 - 1890 (2013/04/10)

To obtain selective and potent inhibitor for T-type calcium channel by ligand based drug design, 2-hydroxy-3-phenoxypropyl piperazine derivatives were synthesized and evaluated for in vitro activities. Compound 6m and 6q showed high selectivity over hERG

Discovery, synthesis, and biological evaluation of piperidinol analogs with anti-tuberculosis activity

Sun, Dianqing,Scherman, Michael S.,Jones, Victoria,Hurdle, Julian G.,Woolhiser, Lisa K.,Knudson, Susan E.,Lenaerts, Anne J.,Slayden, Richard A.,McNeil, Michael R.,Lee, Richard E.

experimental part, p. 3588 - 3594 (2009/10/10)

Direct anti-tuberculosis screening of commercially available compound libraries identified a novel piperidinol with interesting anti-tuberculosis activity and drug like characteristics. To generate a structure activity relationship about this hit a 22 mem

Discovery of para-alkylthiophenoxyacetic acids as a novel series of potent and selective PPARδ agonists

Zhang, Rui,Wang, Aihua,DeAngelis, Alan,Pelton, Patricia,Xu, Jun,Zhu, Peifang,Zhou, Lubing,Demarest, Keith,Murray, William V.,Kuo, Gee-Hong

, p. 3855 - 3859 (2008/02/13)

A novel series of potent and selective PPARδ agonists, para-alkylthiophenoxyacetic acids, was identified. The synthesis and structure-activity relationships are described.

4-((PHENOXYALKYL)THIO)-PHENOXYACETIC ACIDS AND ANALOGS

-

Page/Page column 76, (2010/02/11)

The invention features 4-((phenoxyalkyl)thio)-phenoxyacetic acids and analogs, compositions containing them, and methods of using them as PPAR delta modulators to treat or inhibit the progression of, for example, dyslipidemia.

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