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"Acetic acid, (4-bromo-2-fluorophenoxy)-, ethyl ester" is a complex organic compound with the chemical formula C9H8BrFO3. It is an ester derivative of acetic acid, where the hydroxyl group is replaced by an ethoxy group. The phenoxy group in Acetic acid, (4-bromo-2-fluorophenoxy)-, ethyl ester is substituted with a bromine atom at the 4-position and a fluorine atom at the 2-position. Acetic acid, (4-bromo-2-fluorophenoxy)-, ethyl ester is characterized by its unique structure, which combines the properties of acetic acid, phenol, and halogenated compounds. It is typically synthesized for use in chemical research and as an intermediate in the production of pharmaceuticals and agrochemicals. Due to its specific functional groups, it may exhibit reactivity with nucleophiles and electrophiles, making it a versatile building block in organic synthesis.

1716-83-2

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1716-83-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1716-83-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,1 and 6 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1716-83:
(6*1)+(5*7)+(4*1)+(3*6)+(2*8)+(1*3)=82
82 % 10 = 2
So 1716-83-2 is a valid CAS Registry Number.

1716-83-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-(4-bromo-2-fluorophenoxy)acetate

1.2 Other means of identification

Product number -
Other names <2-Fluor-4-brom-phenoxy>-essigsaeure-aethylester

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:1716-83-2 SDS

1716-83-2Upstream product

1716-83-2Relevant academic research and scientific papers

AMINO ALCOHOL DERIVATIVE, MEDICINAL COMPOSITION CONTAINING THE SAME, AND USE OF THESE

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Page/Page column 38-39, (2008/06/13)

The present invention provides compounds represented by general formula (I): a prodrug thereof, or pharmaceutical acceptable salts thereof, wherein R1 is hydrogen or lower alkyl; each of R2 and R3 is independently hydrogen or lower alkyl; each of R4, R5 and R6 is independently hydrogen, halogen, lower alkyl or lower alkoxy; R7 is hydrogen or lower alkyl; R8 is hydrogen, halogen, lower alkyl, lower alkoxy, etc; R9 is -COR10, -A1-COR10, -O-A2-COR10, etc; Ar is optionally substituted phenyl or heteroaryl; and A is a bond, -OCH2-, etc, which exhibit potent and selective β3-adrenoceptor stimulating activities. The present invention also provides pharmaceutical compositions containing said compound, and uses thereof.

AMINO ALCOHOL DERIVATIVES, PHARMACEUTICAL COMPOSITIONS CONTAINING THE SAME, AND USE THEREOF

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Page/Page column 31, (2008/06/13)

The present invention provides compounds represented by general formula (I): or pharmaceutical acceptable salts thereof, wherein R1 and R2 are each hydrogen or lower alkyl; R3 R4, R5 and R6 are each hydrogen, halogen, lower alkyl or lower alkoxy; R7 and R8 are each hydrogen, halogen, lower alkyl, halo-lower alkyl, lower alkoxy, cycloalkyl, aryl, heteroaryl, cyano, a hydroxyl group, lower acyl, carboxy or the like; R9 is -C(O)-R10, -A1-C(O)-R10, -O-A2-C(O)-R10 or a tetrazol-5-yl group, which exhibit potent and selective β3-adrenoceptor stimulating activities. The present invention also provides pharmaceutical compositions containing said compound, and uses thereof.

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