130203-52-0 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule. In this case, 1,2-Undecanediol, 11-bromoconsists of 11 carbon (C) atoms, 24 hydrogen (H) atoms, 2 oxygen (O) atoms, and 1 bromine (Br) atom.
Explanation
Aliphatic diols are a class of organic compounds that contain two hydroxyl (OH) groups. 1,2-Undecanediol, 11-bromobelongs to this class, as it has two hydroxyl groups attached to a carbon chain.
Explanation
The presence of a bromine atom in the molecular structure of 1,2-Undecanediol, 11-bromodistinguishes it from other aliphatic diols and contributes to its unique properties.
Explanation
Due to its chemical structure, 1,2-Undecanediol, 11-bromois used in various industrial applications, including the production of surfactants and emulsifiers, which are essential in the formulation of various products. It also serves as a chemical intermediate in the synthesis of other compounds.
Explanation
The properties of 1,2-Undecanediol, 11-bromomake it a useful component in the formulation of personal care products, such as cosmetics and toiletries.
Explanation
1,2-Undecanediol, 11-bromocan be used as a potential building block in the synthesis of pharmaceutical compounds, contributing to the development of new drugs.
Explanation
Like other brominated compounds, 1,2-Undecanediol, 11-bromoshould be handled with care due to its potential toxicity and environmental impact. Proper handling and disposal are necessary to minimize any negative effects on the environment.
Explanation
Due to its potential toxicity and environmental impact, it is essential to follow safety precautions when handling 1,2-Undecanediol, 11-bromo-. This includes using appropriate personal protective equipment (PPE) and following proper disposal procedures.
Class
Aliphatic diols
Bromine atom
Contains one bromine atom
Industrial applications
Production of surfactants, emulsifiers, and as a chemical intermediate
Use in personal care products
Formulation component
Use in pharmaceuticals
Potential building block
Environmental impact
Potential toxicity and environmental concerns
Safety precautions
Handle with care
Check Digit Verification of cas no
The CAS Registry Mumber 130203-52-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,2,0 and 3 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 130203-52:
(8*1)+(7*3)+(6*0)+(5*2)+(4*0)+(3*3)+(2*5)+(1*2)=60
60 % 10 = 0
So 130203-52-0 is a valid CAS Registry Number.
130203-52-0Relevant articles and documents
New prodrugs of Adefovir and Cidofovir
Tichy, Tomá?,Andrei, Graciela,Dra?ínsky, Martin,Holy, Antonín,Balzarini, Jan,Snoeck, Robert,Kre?merová, Marcela
, p. 3527 - 3539 (2011)
New Adefovir (PMEA) prodrugs with a pro-moiety consisting of decyl or decyloxyethyl chain bearing hydroxyl function(s), hexaethyleneglycol or a (5-methyl-2-oxo-1,3-dioxolen-4-yl)methyl unit were prepared starting from the tetrabutylammonium salt of the phosphonate drug and an appropriate alkyl bromide or tosylate. Analogously, two esters of Cidofovir [(S)-HPMPC] bearing a hexaethyleneglycol moiety were prepared. The activity of the prodrugs was evaluated in vitro against different virus families. A loss in the antiviral activities of the hydroxylated decyl or decyloxyethyl esters and hexaethyleneglycol esters of PMEA against human immunodeficiency virus (HIV) and herpesviruses [including herpes simplex virus (HSV), varicella-zoster virus (VZV), and human cytomegalovirus (CMV)] occurred in comparison with the parent compound. On the other hand, the (5-methyl-2-oxo-1,3-dioxolen-4-yl)methyl ester of PMEA showed significant activities against HIV and herpesviruses. (S)-HPMPC prodrugs exhibited anti-cytomegalovirus activities in the same range as the parent drug, whereas the anti-HSV and anti-VZV activities were one- to seven-fold lower than that of Cidofovir.
Novel developing agents for (photo) thermographic systems
-
, (2008/06/13)
A thermographic element comprising in a non-aqueous binder medium a silver salt oxidising agent in reactive association with a compound comprising a plurality of redox colour releasing moieties such that oxidation of each redox colour releasing moiety causes release from said compound of a thermally diffusible dye. The compounds many of which are new incorporate two or more developer moieties into a single molecule to minimise the diffusibility of the compound. Following oxidation, either directly by the silver salt or by means of a cross-oxidising agent, each oxidised developer moiety releases a thermally diffusible dye. The compounds are of sufficient size and molecular weight to slow or prevent diffusion in imaging systems and yet possess several active developer moieties per molecule which is advantageous over known ballasted dye releasers which comprise bulky molecules with only a single developer moiety.
