1261475-45-9 Usage
Description
(3-Bromo-2-nitrophenyl)methanol is a chemical compound with the molecular formula C7H6BrNO4. It is a pale yellow solid with a molecular weight of 228.03 g/mol. (3-Bromo-2-nitrophenyl)methanol is known for its ability to undergo various chemical reactions, such as nucleophilic substitution and reduction, making it a versatile building block in the synthesis of pharmaceuticals and agrochemicals.
Uses
Used in Pharmaceutical Industry:
(3-Bromo-2-nitrophenyl)methanol is used as a building block for the synthesis of various pharmaceuticals due to its ability to undergo chemical reactions. It serves as a starting material for the preparation of functionalized compounds with potential biological activities, contributing to the development of new drugs.
Used in Agrochemical Industry:
(3-Bromo-2-nitrophenyl)methanol is also used as a building block in the synthesis of agrochemicals. Its reactivity allows for the creation of compounds with potential applications in agriculture, such as pesticides or herbicides.
Used in Organic Chemistry Research:
In the field of organic chemistry, (3-Bromo-2-nitrophenyl)methanol may be used as a starting material for the study and development of new synthetic methodologies. Its versatility in undergoing chemical reactions makes it a valuable compound for advancing the understanding of organic synthesis processes.
Check Digit Verification of cas no
The CAS Registry Mumber 1261475-45-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,1,4,7 and 5 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1261475-45:
(9*1)+(8*2)+(7*6)+(6*1)+(5*4)+(4*7)+(3*5)+(2*4)+(1*5)=149
149 % 10 = 9
So 1261475-45-9 is a valid CAS Registry Number.
1261475-45-9Relevant articles and documents
A 3 - bromo -2 - nitrobenzaldehyde chemical synthesis method
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Paragraph 0024; 0031-0032; 0043; 0054, (2018/07/15)
The invention relates to a chemical synthesis method of 3-bromo-2-nitrobenzaldehyde. The chemical synthesis method is characterized by using 1,3-dibromo-2-nitrobenzene as a raw material and carrying out five-step reactions including substitution, decarboxylation, oxidation, reduction and hydroformylation, and comprises the following steps of adding 1,3-dibromo-2-nitrobenzene, dimethyl malonate and alkali to an organic solvent to react to prepare 2-(3-bromo-2-nitrobenzaldehyde)-dimethyl malonate; dissolving 2-(3-bromo-2-nitrobenzaldehyde)-dimethyl malonate obtained in the former step in a tetrahydrofuran or acetone solvent, and adding a hydrochloric acid solution to react to prepare 2-(3-bromo-2-nitrobenzaldehyde)-acetic acid; adding a sodium hydroxide water solution and potassium permanganate to react to obtain 3-bromo-2-nitrobenzoic acid; dissolving 3-bromo-2-nitrobenzoic acid in the tetrahydrofuran solvent, and adding borane tetrahydrofuran to react to obtain 3-bromo-2-nitrobenzyl alcohol; adding 3-bromo-2-nitrobenzyl alcohol to a dichloromethane or 1,2-dichloroethane solvent and adding manganese dioxide to react to prepare 3-bromo-2-nitrobenzaldehyde. The synthetic route has the advantages of low cost and high yield.
Tunable emissive thin films through ICT photodisruption of nitro-substituted triarylamines
Jacquart, Aurelie,Tauc, Patrick,Pansu, Robert B.,Ishow, Elena
supporting information; experimental part, p. 4360 - 4362 (2010/08/22)
UV-assisted photocleavage in the solid state of orange emitting nitro-substituted triarylamines leads to the appearance of blue emission following photodisruption of the ICT state.
