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2-Fluoro-3-Nitrobenzaldehyde is a chemical compound characterized by the molecular formula C7H4FNO3. It is an organic compound that features both a fluorine atom and a nitro group attached to a benzene ring, making it a versatile building block in the synthesis of various organic compounds.

96516-29-9

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96516-29-9 Usage

Uses

Used in Pharmaceutical Industry:
2-Fluoro-3-Nitrobenzaldehyde is utilized as a key intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of new drugs with specific therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical sector, 2-Fluoro-3-Nitrobenzaldehyde is employed as a precursor in the production of agrochemicals, which are essential for enhancing crop protection and yield.
Used in Dye Industry:
2-Fluoro-3-Nitrobenzaldehyde serves as a crucial component in the creation of dyes, where its unique structure contributes to the color and properties of the final product.
Used as a Fluorescent Probe in Environmental Analysis:
2-Fluoro-3-Nitrobenzaldehyde has demonstrated its potential as a fluorescent probe for detecting heavy metal ions in environmental samples, offering a valuable tool for environmental monitoring and protection.

Check Digit Verification of cas no

The CAS Registry Mumber 96516-29-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,5,1 and 6 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 96516-29:
(7*9)+(6*6)+(5*5)+(4*1)+(3*6)+(2*2)+(1*9)=159
159 % 10 = 9
So 96516-29-9 is a valid CAS Registry Number.
InChI:InChI=1/C7H4FNO3/c8-7-5(4-10)2-1-3-6(7)9(11)12/h1-4H

96516-29-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Fluoro-3-nitrobenzaldehyde

1.2 Other means of identification

Product number -
Other names 2-FLUORO-3-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:96516-29-9 SDS

96516-29-9Relevant articles and documents

CONDENSED BI-HETEROCYCLES AS INHIBITING AGENTS FOR BRUTON'S TYROSINE KINASE

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Page/Page column 120, (2021/05/07)

Provided are compounds of Formula (I): Formula (I) or pharmaceutically acceptable salts thereof, wherein R1, R2, R3, R4, R5, R6, A1, B1, B2, Q1 and Q2 are as defined herein; and methods for their use and production.

INHIBITING AGENTS FOR BRUTON'S TYROSINE KINASE

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Page/Page column 154, (2019/12/04)

Provided are compounds of Formula (I), or pharmaceutically acceptable salts thereof, methods for use as Bruton's tyrosine kinase and methods of production.

Nitration of Strongly Deactivated Aromatics with Superacidic Mixed Nitric-Triflatoboric Acid (HNO3/2CF3SO3H-B(O3SCF3)3)

Olah, George A.,Orlinkov, Alexander,Oxyzoglou, Alexandros B.,Prakash, G. k. Surya

, p. 7348 - 7350 (2007/10/03)

The nitration of various deactivated arenes (including methanesulfonyl-, nitro-, and polyhalobenzenes) was carried out in good yield with mixed nitric-triflatoboric superacid.For example pentafluorobenzene gave pentafluoronitrobenzene in 99percent yield, nitrobenzene to m-dinitrobenzene in 92percent selectivity with 85percent overall yield, and methyl phenyl sulfone gave only the m-nitro isomer in 78percent isolated yield.Thus the new nitrating system gives high regioselectivity and yields under generally mild reaction conditions.The reagent system is compatible with many functional groups of arenes.

Synthesis and antihypertensive activity of 1,4-dihydropyridine derivatives with a 4-(disubstituted phenyl) ring and an aminoalkyl ester group: Highly potent and long-lasting calcium antagonists

Kanno,Yamaguchi,Okamiya,Sunakawa,Takeshita,Naruchi

, p. 2049 - 2054 (2007/10/02)

New 1,4-dihydropyridine derivatives bearing a 4-(disubstituted phenyl) ring and an aminoethyl ester or an amino-2,2-dimethylpropyl ester were synthesized and their antihypertensive activities were examined in normotensive rats and spontaneously hypertensi

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