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3-Fluoro-5-nitrobenzaldehyde is an organic compound characterized by the presence of a nitro group (-NO2) at the 5th position and a fluorine atom (-F) at the 3rd position on a benzene ring, with an aldehyde (-CHO) functional group attached to the carbon at the 1st position. 3-fluoro-5-nitrobenzaldehyde is known for its reactivity and is commonly utilized in the synthesis of various organic molecules.

108159-96-2

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108159-96-2 Usage

Uses

Used in Pharmaceutical Industry:
3-fluoro-5-nitrobenzaldehyde is used as a reactant for the design and synthesis of selective activators of cardiac myosin. These activators play a crucial role in enhancing the contractile function of the heart, which can be beneficial in the treatment of certain heart conditions and improving cardiac performance.

Check Digit Verification of cas no

The CAS Registry Mumber 108159-96-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,1,5 and 9 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 108159-96:
(8*1)+(7*0)+(6*8)+(5*1)+(4*5)+(3*9)+(2*9)+(1*6)=132
132 % 10 = 2
So 108159-96-2 is a valid CAS Registry Number.

108159-96-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Fluoro-5-Nitrobenzaldehyde

1.2 Other means of identification

Product number -
Other names 3-Fluoro-5-nitrobenzaldehyde

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:108159-96-2 SDS

108159-96-2Relevant academic research and scientific papers

Compounds, Compositions and Methods

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Page/Page column 16, (2009/08/14)

Certain substituted urea derivatives modulate the cardiac sarcomere, for example by potentiating cardiac myosin, and are useful in the treatment of systolic heart failure including congestive heart failure.

Elemental fluorine. Part 21. (1) direct fluorination of benzaldehyde derivatives

Chambers, Richard D.,Sandford, Graham,Trmcic, Jelena,Okazoe, Takashi

, p. 339 - 344 (2013/01/03)

Direct fluorination of a range of benzaldehyde derivatives gives mixtures of fluorobenzaldehyde and benzoyl fluoride products in ratios that depend upon the nature of the ring substituent Electron-withdrawing substituents give predominantly benzoyl fluoride derivatives, whereas electron-donating substituents lead to fluoroarene systems. Separation of ring-fluorinated products can be easily accomplished by esterification of the benzoyl fluoride side products. Scale-up of these processes to provide significant quantities of appropriate fluorobenzaldehyde systems has also been achieved using continuous flow techniques.

CERTAIN CHEMICAL ENTITIES, COMPOSITIONS AND METHODS

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Page/Page column 40, (2010/11/27)

Certain substituted urea derivatives selectively modulate the cardiac sarcomere, for example by potentiating cardiac myosin, and are useful in the treatment of systolic heart failure including congestive heart failure.

CERTAIN CHEMICAL ENTITIES, COMPOSITIONS AND METHODS

-

Page/Page column 83, (2010/11/27)

Certain substituted urea derivatives selectively modulate the cardiac sarcomere, for example by potentiating cardiac myosin, and are useful in the treatment of systolic heart failure including congestive heart failure.

Compounds, compositions and methods

-

Page/Page column 29, (2008/06/13)

Certain substituted urea derivatives selectively modulate the cardiac sarcomere, for example by potentiating cardiac myosin, and are useful in the treatment of systolic heart failure including congestive heart failure.

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