26049-98-9 Usage
Uses
Used in Pharmaceutical Industry:
ZPCK is used as an active ingredient in medicated shampoos and topical treatments for managing fungal and bacterial overgrowth on the scalp. It is particularly effective against conditions like dandruff and seborrheic dermatitis, providing relief and promoting a healthy scalp environment.
Used in Dermatology:
ZPCK is used as a key component in dermatological formulations recommended by dermatologists for the treatment of scalp issues. Its multifaceted action against fungi and bacteria makes it a valuable tool in maintaining skin health and addressing specific scalp conditions effectively.
Used in Personal Care Industry:
ZPCK is used as an ingredient in anti-dandruff shampoos and other hair care products to combat dandruff and promote overall scalp health. Its inclusion in these products helps to reduce flaking, itching, and irritation associated with fungal or bacterial overgrowth on the scalp.
Used in Antifungal Treatments:
ZPCK is used as a potent antifungal agent in various treatments aimed at eradicating fungal infections on the skin. The combination of its components ensures a comprehensive approach to tackling fungal overgrowth, making it a preferred choice for treating conditions caused by such infections.
Check Digit Verification of cas no
The CAS Registry Mumber 26049-98-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,0,4 and 9 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 26049-98:
(7*2)+(6*6)+(5*0)+(4*4)+(3*9)+(2*9)+(1*8)=119
119 % 10 = 9
So 26049-98-9 is a valid CAS Registry Number.
InChI:InChI=1/C18H18ClNO3/c19-12-17(21)16(11-14-7-3-1-4-8-14)20-18(22)23-13-15-9-5-2-6-10-15/h1-10,16H,11-13H2,(H,20,22)
26049-98-9Relevant academic research and scientific papers
PROCESS FOR THE PREPARATION OF ALPHA-CHLOROKETONES FROM ALKYL ESTERS
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Page/Page column 6-7, (2010/02/11)
The present invention relates to a process for the preparation of α-chloroketones from readily available alkyl esters by the reaction of a sulfoxonium ylide on said alkyl esters to generate a keto sulfoxonium ylide that is in turn treated with anhydrous HCl.
Processes for producing α-halo ketones, α-halohydrins and epoxides
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, (2008/06/13)
Processes for efficiently producing α-halo ketones, α-halohydrins and epoxides on an industrial scale. The prosesses include one for producing an α-halo ketone of general formula (3) by decarboxylating a product of reaction between a carboxilic acid derivative of general formula (1) and a metal enolate prepared from an α-haloacetic acid of general formula (2) or an acceptable salt thereof, one for producing an by reducing the α-halo ketone (3), and one for producing an epoxide (13) by treating the α-halohydrin (11) with a base to effect ring closure. The above prosesses are particularly suitable for producing optically active α-halo ketones, α-halohydrins and epoxides from the corresponding α-amino acid derivatives. STR1
