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C9H8BrFO2, a chemical compound with the molecular formula C9H8BrFO2, is a member of the phenylpropanoic acids class. It is composed of carbon, hydrogen, bromine, fluorine, and oxygen atoms, featuring a phenyl group attached to a propanoic acid. This versatile organic compound exhibits significant chemical reactivity and biological activity.

1204304-98-2

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1204304-98-2 Usage

Uses

Used in Pharmaceutical Industry:
C9H8BrFO2 serves as an intermediate in the synthesis of pharmaceutical drugs. Its unique structure and reactivity allow for the development of various medicinal compounds, contributing to the advancement of drug discovery and therapeutic applications.
Used in Agrochemical Industry:
C9H8BrFO2 is also utilized as an intermediate in the production of agrochemicals. Its chemical properties make it suitable for the creation of compounds that can be used in agriculture to enhance crop protection and productivity.

Check Digit Verification of cas no

The CAS Registry Mumber 1204304-98-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,4,3,0 and 4 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1204304-98:
(9*1)+(8*2)+(7*0)+(6*4)+(5*3)+(4*0)+(3*4)+(2*9)+(1*8)=102
102 % 10 = 2
So 1204304-98-2 is a valid CAS Registry Number.

1204304-98-2Downstream Products

1204304-98-2Relevant academic research and scientific papers

Exploration of O-spiroketal C-arylglucosides as novel and selective renal sodium-dependent glucose co-transporter 2 (SGLT2) inhibitors

Lv, Binhua,Xu, Baihua,Feng, Yan,Peng, Kun,Xu, Ge,Du, Jiyan,Zhang, Lili,Zhang, Wenbin,Zhang, Ting,Zhu, Liangcheng,Ding, Haifeng,Sheng, Zelin,Welihinda, Ajith,Seed, Brian,Chen, Yuanwei

scheme or table, p. 6877 - 6881 (2010/05/19)

A series of novel O-spiroketal C-arylglucosides have been prepared and evaluated in cell-based functional assays for activity against human sodium-dependent glucose co-transporters 1 and 2 (SGLT1 and 2). The core spiro[isobenzofuran-1,2′-pyran] structure proved to be an effective scaffold for diversification and a number of compounds with single digit nanomolar potency and high selectivity have been synthesized. Compound 5a promoted glucosuria when administered in vivo in rats and produced a significant blood glucose reduction effect.

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