26018-44-0 Usage
Description
(7-Chloro-2,3-dihydrobenzofuran-2-yl)Methanol, also known as 7-chloro-2,3-dihydro-2-benzofuranylmethanol, is a chemical compound with a molecular formula C9H9ClO2. It is a white solid at room temperature and is used in the synthesis of pharmaceuticals and other organic compounds. (7-Chloro-2,3-dihydrobenzofuran-2-yl)Methanol is important in the field of medicinal chemistry and drug discovery, as it can be used as a building block for the creation of various biologically active molecules.
Uses
Used in Pharmaceutical Industry:
(7-Chloro-2,3-dihydrobenzofuran-2-yl)Methanol is used as a building block for the creation of various biologically active molecules, contributing to the development of new pharmaceuticals and other bioactive compounds.
Used in Pesticide Production:
(7-Chloro-2,3-dihydrobenzofuran-2-yl)Methanol is used in the production of pesticides, playing a role in the development of effective and safe agrochemicals.
Used in Dye Industry:
(7-Chloro-2,3-dihydrobenzofuran-2-yl)Methanol is used in the production of dyes, contributing to the creation of a wide range of colorants for various applications.
Used in Perfume Industry:
(7-Chloro-2,3-dihydrobenzofuran-2-yl)Methanol is used in the production of perfumes, adding to the development of fragrances and scents for personal and commercial use.
Used in Medicinal Research and Development:
(7-Chloro-2,3-dihydrobenzofuran-2-yl)Methanol is important for the study and development of new pharmaceuticals and other bioactive compounds, making it a valuable chemical in the field of medicinal research and development.
Check Digit Verification of cas no
The CAS Registry Mumber 26018-44-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,0,1 and 8 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 26018-44:
(7*2)+(6*6)+(5*0)+(4*1)+(3*8)+(2*4)+(1*4)=90
90 % 10 = 0
So 26018-44-0 is a valid CAS Registry Number.
26018-44-0Relevant articles and documents
Enantioselective acylation of 2-hydroxymethyl-2,3-dihydrobenzofurans catalysed by lipase from Pseudomonas cepacia (Amano PS) and total stereoselective synthesis of (-)-(R)-MEM-protected arthrographol
Ramadas,Krupadanam, G. L. David
, p. 3375 - 3393 (2007/10/03)
Lipase Amano PS catalysed acylation of (±)-2-hydroxymethyl-2,3-dihydrobenzofurans using vinyl acetate as the acyl donor in n-hexane gave (-)-(R)-2-acetoxymethyl-2,3-dihydrobenzofurans and (+)-(S)-2-hydroxymethyl-2,3-dihydrobenzofurans in high enantiomeric excess. (-)-(R)-Acetate 18j is converted to (-)-(R)-MEM-protected arthrographol 22. Copyright (C) 2000 Elsevier Science Ltd.
