18362-30-6 Usage
General Description
2-Chloro-6-hydroxybenzaldehyde is a type of chemical compound prevalent in the field of organic chemistry. It has a chlorine atom and a hydroxy group attached to a benzaldehyde base. This makes it highly reactive and suitable for various chemical reactions. 2-CHLORO-6-HYDROXYBENZALDEHYDE is often used as a precursor or intermediate in the synthesis of other more complex molecules. It displays the typical characteristics of an aromatic aldehyde, and its properties of a slight solubility in water and ability to create crystals make it valuable for specific types of research and development. Its exact properties can vary depending on factors like temperature, pressure, and presence of other substances.
Check Digit Verification of cas no
The CAS Registry Mumber 18362-30-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,3,6 and 2 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 18362-30:
(7*1)+(6*8)+(5*3)+(4*6)+(3*2)+(2*3)+(1*0)=106
106 % 10 = 6
So 18362-30-6 is a valid CAS Registry Number.
InChI:InChI=1/C7H5ClO2/c8-6-2-1-3-7(10)5(6)4-9/h1-4,10H
18362-30-6Relevant articles and documents
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Bunnett et al.
, p. 2512,2513 (1961)
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Postmus,C. et al.
, p. 2693 - 2698 (1964)
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PROCESS FOR PREPARING 3-CHLORO-2-VINYLPHENYLSULFONATES
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, (2018/04/14)
The present invention relates to a new process for preparing 3-chloro-2-vinylphenylsulfonate derivatives.
Pd-Catalyzed Ortho C-H Hydroxylation of Benzaldehydes Using a Transient Directing Group
Chen, Xiao-Yang,Ozturk, Seyma,Sorensen, Erik J.
supporting information, p. 6280 - 6283 (2017/12/08)
The direct Pd-catalyzed ortho C-H hydroxylation of benzaldehydes was achieved using 4-chloroanthranilic acid as the transient directing group, 1-fluoro-2,4,6-trimethylpyridnium triflate as the bystanding oxidant, and p-toluenesulfonic acid as the putative oxygen nucleophile. The unusual C-H chlorination and polyfluoroalkoxylation reactions signaled the importance of external nucleophiles to the outcome of Pd(IV) reductive eliminations.