23602-61-1 Usage
Description
3,4-Dichloro-2-hydroxybenzaldehyde is a chemical compound characterized by its molecular formula C7H4Cl2O2. It is a white to light yellow solid with a distinctive aromatic odor. 3,4-Dichloro-2-hydroxybenzaldehyde is recognized for its solubility in organic solvents such as ethanol and acetone, and its structure, which includes chloro and hydroxy groups, makes it a valuable building block in the synthesis of a variety of organic compounds. However, due to its potential to irritate the skin, eyes, and respiratory system, it requires careful handling.
Uses
Used in Pharmaceutical Synthesis:
3,4-Dichloro-2-hydroxybenzaldehyde is utilized as an intermediate in the production of pharmaceuticals. Its unique structure allows it to be a key component in the synthesis of various medicinal compounds, contributing to the development of new drugs and therapies.
Used in Agrochemical Production:
3,4-Dichloro-2-hydroxybenzaldehyde also serves as an intermediate in the synthesis of agrochemicals. Its role in this industry is crucial for the development of substances used in agriculture to protect crops and enhance yields.
Used in Dye and Pigment Manufacturing:
3,4-Dichloro-2-hydroxybenzaldehyde is used as an intermediate in the production of dyes and pigments. Its chemical properties make it suitable for creating a range of colors used in various industries, including textiles, plastics, and printing.
Used in Organic Synthesis:
Due to its versatility, 3,4-Dichloro-2-hydroxybenzaldehyde is a valuable intermediate in organic synthesis. It is employed in the creation of a wide array of organic compounds for different applications across various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 23602-61-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,6,0 and 2 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 23602-61:
(7*2)+(6*3)+(5*6)+(4*0)+(3*2)+(2*6)+(1*1)=81
81 % 10 = 1
So 23602-61-1 is a valid CAS Registry Number.
23602-61-1Relevant articles and documents
Extending the stetter reaction with 1,6-acceptors
Law, Katherine R.,McErlean, Christopher S. P.
supporting information, p. 15852 - 15855 (2014/04/03)
Pace Stetter: A new N-heterocyclic carbene (NHC)-catalysed transformation is described-the intramolecular vinylogous Stetter reaction. This transformation can be effected with both thiazolium and triazolium-based catalysts, using aromatic and aliphatic aldehydes, employing α,β,γ,δ- unsaturated esters, ketones, phosphonates and N-acylpyrroles, and can be conducted enantioselectively (see scheme). Copyright
Salicylaldoxime moiety as a phenolic "A-ring" substitute in estrogen receptor ligands
Minutolo,Bertini,Papi,Carlson,Katzenellenbogen,Macchia
, p. 4288 - 4291 (2007/10/03)
The phenolic "A-ring" of natural and synthetic estrogen receptor (ER) ligands was effectively replaced by a planar six-member ring formed through an intramolecular hydrogen bond within a salicylaldoxime. Thus, oxime 1, a structural analogue of a triarylet
