675872-43-2 Usage
Description
(3,5-dibromothiophen-2-yl)methanol is a chemical compound that belongs to the family of organobromides and thioethers. It is a white to off-white solid with a molecular formula C6H5Br2OS and a molecular weight of 264.98 g/mol. (3,5-dibroMothiophen-2-yl)Methanol is known for its potential use in the synthesis of pharmaceuticals, agrochemicals, polymers, and other organic compounds. It also serves as a building block for creating various chemical structures and exhibits biological activity.
Uses
Used in Pharmaceutical Industry:
(3,5-dibromothiophen-2-yl)methanol is used as a key intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of new drugs with potential therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical industry, (3,5-dibromothiophen-2-yl)methanol is utilized as a precursor in the production of agrochemicals, which can help in the development of effective pesticides and other agricultural chemicals.
Used in Polymer Production:
(3,5-dibromothiophen-2-yl)methanol is employed as a monomer or building block in the production of polymers, contributing to the creation of materials with specific properties for various applications.
Used in Organic Synthesis:
As a versatile chemical compound, (3,5-dibromothiophen-2-yl)methanol is used in organic synthesis for the creation of a wide range of organic compounds, expanding the scope of chemical research and development.
Check Digit Verification of cas no
The CAS Registry Mumber 675872-43-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,7,5,8,7 and 2 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 675872-43:
(8*6)+(7*7)+(6*5)+(5*8)+(4*7)+(3*2)+(2*4)+(1*3)=212
212 % 10 = 2
So 675872-43-2 is a valid CAS Registry Number.
675872-43-2Relevant articles and documents
Preparation method of hydroxymethyl-substituted aromatic heterocyclic compound
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Paragraph 0049-0055, (2020/08/02)
The invention provides a preparation method of a hydroxymethyl-substituted aromatic heterocyclic compound, which comprises the following steps: in the presence of protective gas, dissolving aromatic heterocarboxylic acid in an aprotic solvent, adding a reducing agent in an ice bath, performing heating to room temperature, and performing reacting to obtain the hydroxymethyl-substituted aromatic heterocyclic compound. The yield of the hydroxymethyl substituted aromatic heterocyclic compound is 93% or above, the raw materials are cheap and easy to obtain, the method is simple, efficient and mildin reaction condition, and the defect that dangerous chemicals such as sodium borohydride which are prone to explosion are used in a conventional synthesis method can be overcome.
Construction of Arene-Fused-Piperidine Motifs by Asymmetric Addition of 2-Trityloxymethylaryllithiums to Nitroalkenes: The Asymmetric Synthesis of a Dopamine D1 Full Agonist, A-86929
Yamashita, Mitsuaki,Yamada, Ken-Ichi,Tomioka, Kiyoshi
, p. 1954 - 1955 (2007/10/03)
The straightforward methodology for the construction of chiral arene-fused-piperidine motifs using a highly enantioselective addition of 2-trityloxymethylaryllithiums to cyclic and acyclic nitroalkenes has been developed. The versatility of the process wa
