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"Acetic acid, (2-bromo-4-fluorophenoxy)-, ethyl ester" is a chemical compound with the molecular formula C9H8BrFO3. It is an ester derivative of acetic acid, where the hydroxyl group is replaced by an ethoxy group, and the phenyl ring is substituted with a bromine atom at the 2nd position and a fluorine atom at the 4th position. Acetic acid, (2-bromo-4-fluorophenoxy)-, ethyl ester is characterized by its unique structure, which contributes to its specific chemical properties and potential applications in various fields, such as pharmaceuticals or agrochemicals. It is important to note that handling and usage of Acetic acid, (2-bromo-4-fluorophenoxy)-, ethyl ester should be done with caution, as it may have specific safety and environmental considerations.

1842-10-0

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1842-10-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1842-10-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,4 and 2 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1842-10:
(6*1)+(5*8)+(4*4)+(3*2)+(2*1)+(1*0)=70
70 % 10 = 0
So 1842-10-0 is a valid CAS Registry Number.

1842-10-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

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

1.2 Other means of identification

Product number -
Other names ethyl (2-bromo-4-fluorophenoxy)acetate

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:1842-10-0 SDS

1842-10-0Downstream Products

1842-10-0Relevant academic research and scientific papers

INHIBITORS OF THE MENIN-MLL INTERACTION

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Page/Page column 77; 114, (2018/01/17)

The present invention is directed to inhibitors of the interaction of menin with MLL and MLL fusion proteins, pharmaceutical compositions containing the same, and their use in the treatment of cancer and other diseases mediated by the menin-MLL interaction.

BIPHENYLOXYACETIC ACID DERIVATIVES FOR THE TREATMENT OF RESPIRATORY DISEASE

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Page/Page column 36, (2008/06/13)

The invention relates to substituted phenoxyacetic acids of formula (I), where the variables are as defined in claim 1, as useful pharmaceutical compounds for treating respiratory disorders, pharmaceutical compositions containing them, and processes for their preparation.

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