96516-29-9 Usage
General Description
2-Fluoro-3-Nitrobenzaldehyde is a chemical compound with the molecular formula C7H4FNO3. It is an organic compound that contains both fluorine and nitro groups attached to a benzene ring. 2-Fluoro-3-Nitrobenzaldehyde is widely used in the pharmaceutical and chemical industries as a building block for the synthesis of various organic compounds. It is specifically used in the production of agrochemicals, pharmaceuticals, and dyes. Additionally, 2-Fluoro-3-Nitrobenzaldehyde has shown potential as a fluorescent probe for detecting heavy metal ions in environmental samples. It is important to handle this compound with caution as it is toxic if ingested and can cause irritation to the skin, eyes, and respiratory system.
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
96516-29-9Relevant 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.
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.
