19561-95-6 Usage
Description
1-[4-(2-Chloroethoxy)phenyl]-2-phenylethanone, with the CAS number 19561-95-6, is an off-white solid compound that is primarily utilized in the field of organic synthesis. It is a synthetic chemical with a unique molecular structure that contributes to its various applications in chemical reactions and the formation of new compounds.
Uses
Used in Organic Synthesis:
1-[4-(2-Chloroethoxy)phenyl]-2-phenylethanone is used as a synthetic intermediate for the production of various organic compounds. Its unique structure allows it to participate in a range of chemical reactions, such as substitution, addition, and condensation, which are essential for the synthesis of complex organic molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 1-[4-(2-Chloroethoxy)phenyl]-2-phenylethanone is used as a key building block for the development of new drugs. Its chemical properties make it suitable for the synthesis of various drug candidates, which can be further modified and optimized to exhibit desired pharmacological properties.
Used in Chemical Research:
1-[4-(2-Chloroethoxy)phenyl]-2-phenylethanone is also employed in chemical research as a model compound to study various reaction mechanisms and to develop new synthetic methodologies. Its reactivity and structural features provide valuable insights into the behavior of similar compounds and help researchers design more efficient and selective synthetic routes.
Used in Material Science:
In the field of material science, 1-[4-(2-Chloroethoxy)phenyl]-2-phenylethanone can be used as a precursor to develop novel materials with specific properties. Its chemical structure can be tailored to create materials with unique characteristics, such as improved stability, enhanced reactivity, or specific interactions with other molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 19561-95-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,5,6 and 1 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 19561-95:
(7*1)+(6*9)+(5*5)+(4*6)+(3*1)+(2*9)+(1*5)=136
136 % 10 = 6
So 19561-95-6 is a valid CAS Registry Number.
InChI:InChI=1/C16H15ClO2/c17-10-11-19-15-8-6-14(7-9-15)16(18)12-13-4-2-1-3-5-13/h1-9H,10-12H2
19561-95-6Relevant articles and documents
Novel compounds that reverse the disease phenotype in Type 2 Gaucher disease patient-derived cells
Abou-Gharbia, Magid,Childers, Wayne,Colussi, Dennis J.,Fan, Rong,Gordon, John,Jacobson, Marlene A.,Liu, Yuxiao,Martinez, Rogelio,Melenski, Edward
supporting information, (2019/12/11)
Gaucher disease (GD) results from inherited mutations in the lysosomal enzyme β-glucocerobrosidase (GCase). Currently available treatment options for Type 1 GD are not efficacious for treating neuronopathic Type 2 and 3 GD due to their inability to cross the blood-brain barrier. In an effort to identify small molecules which could be optimized for CNS penetration we identified tamoxifen from a high throughput phenotypic screen on Type 2 GD patient-derived fibroblasts which reversed the disease phenotype. Structure activity studies around this scaffold led to novel molecules that displayed improved potency, efficacy and reduced estrogenic/antiestrogenic activity compared to the original hits. Here we present the design, synthesis and structure activity relationships that led to the lead molecule Compound 31.
Triphenylalkene derivatives and their use as selective estrogen receptor modulators
-
, (2008/06/13)
The invention provides novel selective estrogen receptor modulator compounds of the general formula: wherein R1 and R2, which are the same or different are a) H, halogen, OCH3, OH; or ?where X is O, NH or S; and n is an integer from 1 to 4; and R4 and R5, which are the same or different, are a 1 to 4 carbon alkyl, H, —CH2C≡CH or —CH2CH2OH; or R4 and R5 form an N-containing five- or six-membered ring or heteroaromatic ring; or c) —Y—(CH2)nCH2—O—R6 where Y is O, NH or S and n is an integer from 1 to 4; and R6 is H, —CH2CH2OH, or —CH2CH2Cl; or d) 2,3-dihydroxypropoxy, 2-methylsulfamylethoxy, 2-chloroethoxy, 1-ethyl-2-hydroxyethoxy, 2,2-diethyl-2-hydroxyethoxy or carboxymethoxy; and R3 is H, halogen, OH or —OCH3; stereoisomers thereof and their non-toxic pharmaceutically acceptable salts and esters and mixtures thereof, which compounds exhibit valuable pharmacological properties.
