1006-54-8 Usage
Uses
Used in Pharmaceutical Industry:
Phenol, 2-(bromomethyl)-4,6-dichlorois used as an intermediate in the production of pharmaceuticals for its ability to be synthesized into various medicinal compounds.
Used in Pesticide Industry:
In the pesticide industry, Phenol, 2-(bromomethyl)-4,6-dichloroserves as an intermediate, contributing to the development of effective pest control agents.
Used in Organic Synthesis:
Phenol, 2-(bromomethyl)-4,6-dichlorois utilized in the synthesis of other organic compounds, highlighting its versatility in chemical reactions and product development.
Used in Antiseptic and Disinfectant Applications:
Due to its antiseptic and disinfectant properties, Phenol, 2-(bromomethyl)-4,6-dichloromay be used in medical or laboratory settings to prevent infection and maintain a sterile environment.
Check Digit Verification of cas no
The CAS Registry Mumber 1006-54-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,0 and 6 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1006-54:
(6*1)+(5*0)+(4*0)+(3*6)+(2*5)+(1*4)=38
38 % 10 = 8
So 1006-54-8 is a valid CAS Registry Number.
1006-54-8Relevant articles and documents
2-piperazine ethyl phenyl carbamate derivatives and pharmaceutical application thereof
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Paragraph 0017-0020; 0022, (2020/06/20)
The invention relates to a phenyl 2-piperazine ethyl carbamate derivative and a pharmaceutical application thereof. The structure of the phenyl 2-piperazine ethyl carbamate derivative accords with a general formula (I), wherein R is -H or-CH3. The drug ha
Titanium and zirconium complexes of robust salophan ligands. Coordination chemistry and olefin polymerization catalysis
Gendler, Shimrit,Zelikoff, Ayellet L.,Kopilov, Jacob,Goldberg, Israel,Kol, Moshe
, p. 2144 - 2145 (2008/09/19)
The synthesis of [ONNO]-type robust Salophan ligands featuring tertiary nitrogen donors is described for the first time. By varying the substitution pattern on the aromatic bridge and on the phenolate rings, four ligands possessing a broad scope of electr
