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N-butyl-2-fluoro-4-nitroaniline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

124431-93-2

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124431-93-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 124431-93-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,4,3 and 1 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 124431-93:
(8*1)+(7*2)+(6*4)+(5*4)+(4*3)+(3*1)+(2*9)+(1*3)=102
102 % 10 = 2
So 124431-93-2 is a valid CAS Registry Number.

124431-93-2Downstream Products

124431-93-2Relevant academic research and scientific papers

Tyrosine kinase inhibitor, preparation method and application thereof

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Paragraph 0046; 0047, (2017/01/26)

The invention provides a tyrosine kinase inhibitor having the structure represented as follows, wherein R1 is a halogenated group, R2 is selected from a C1-C6 alkoxy group, a C1-C10 carbonate substituted group, a C1-C6 imino substituted group, or the foll

THE PHOTOREACTIONS OF 2-FLUORO-4-NITROANISOLE WITH AMINES. THE SEARCH FOR NEW BIOCHEMICAL PHOTOPROBES

Figueredo, M.,Marquet, J.,Moreno-Manas, M.,Pleixats, R.

, p. 2427 - 2428 (2007/10/02)

The photosubstitutions of 2-fluoro-4-nitroanisole with several amines are studied from the preparative and the preliminary mechanistic points of view.The possible usefulness of this structure as biochemical photoprobe is discussed.

THE SEARCH FOR NEW BIOCHEMICAL PHOTOPROBES. II. THE NUCLEOPHILIC PHOTOSUBSTITUTION OF 2-FLUORO-4-NITROANISOLE.

Pleixats, R.,Figueredo, M.,Marquet, J.,Moreno-Manas, M.,Cantos, A.

, p. 7817 - 7826 (2007/10/02)

The photosubstitutions of 2-fluoro-4-nitroanisole with several amines are studied.The preparative results, the thermal stability of the photochemical substrate, and the limiting quantum yield values obtained from photoreactions with several nucleophiles suggest the possible usefulness of 2-fluoro-4-nitrophenyl ethers as biochemical photoprobes.

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