134997-67-4 Usage
General Description
2-<(2-chloroacetyl)amino>-4-methylphenol is a chemical compound with the molecular formula C9H10ClNO2. It is a derivative of phenol and contains a chlorine atom and an acetylamine group attached to the phenol ring. 2-<(2-chloroacetyl)amino>-4-methylphenol is commonly used in the pharmaceutical and cosmetic industries for its antimicrobial and antifungal properties. It is also used as an intermediate in the synthesis of other organic compounds and can be found in some antiseptic and anti-inflammatory topical medications. Additionally, it has potential applications in the field of agriculture as a pesticide or herbicide due to its antimicrobial properties. The compound should be handled with care and in accordance with safety regulations due to its potential toxicity and irritant properties.
Check Digit Verification of cas no
The CAS Registry Mumber 134997-67-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,9,9 and 7 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 134997-67:
(8*1)+(7*3)+(6*4)+(5*9)+(4*9)+(3*7)+(2*6)+(1*7)=174
174 % 10 = 4
So 134997-67-4 is a valid CAS Registry Number.
134997-67-4Relevant articles and documents
A novel series of substituted 1,2,3-triazoles as cancer stem cell inhibitors: Synthesis and biological evaluation
Padhariya, Komal N.,Athavale, Maithili,Srivastava, Sangeeta,Kharkar, Prashant S.
, p. 68 - 85 (2021)
An alarming increase in global death toll resulting from cancer incidents, particularly due to multidrug resistance and reduced efficacy as a consequence of target mutations, has compelled us to look for novel anticancer agents. Cancer stem cells (CSCs),
Synthesis and topical antiinflammatory and antiallergic activities of antioxidant o-aminophenol derivatives
Sugiyama,Akahoshi,Kuwahara,Kajii,Sakaue,Yakumaru,Sugiura,Fukaya
, p. 1977 - 1982 (2007/10/02)
In order to develop novel compounds for topical use possessing antiallergic as well as antiinflammatory activities, a series of o- aminophenol derivatives bearing H1-antihistaminic structures were synthesized and their effects were investigated
