113137-29-4 Usage
Description
N-(4-Chloro-6-methoxyphenyl)-2,2-dimethylpropanamide, with the CAS number 113137-29-4, is a chemical compound that is characterized as a brown solid. It is primarily utilized in the field of organic synthesis, where it serves as a valuable intermediate for the creation of various other compounds.
Uses
Used in Organic Synthesis:
N-(4-Chloro-6-methoxyphenyl)-2,2-dimethylpropanamide is used as a synthetic intermediate for the production of other chemical compounds. Its unique structure, which includes a chloro and methoxy group on the phenyl ring, allows for a range of reactions and modifications that can be applied to generate diverse molecules with specific properties and applications.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, N-(4-Chloro-6-methoxyphenyl)-2,2-dimethylpropanamide may be used as a building block for the development of new drugs. Its chemical properties make it a promising candidate for the synthesis of novel molecules with potential therapeutic effects. The compound's reactivity and structural features can be exploited to design drugs targeting specific biological pathways or receptors.
Used in Chemical Research:
N-(4-Chloro-6-methoxyphenyl)-2,2-dimethylpropanamide is also valuable in chemical research, where it can be employed to study various reaction mechanisms and explore new synthetic routes. Researchers can use this compound to gain insights into the behavior of similar molecules and develop innovative strategies for the synthesis of complex organic compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 113137-29-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,1,3 and 7 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 113137-29:
(8*1)+(7*1)+(6*3)+(5*1)+(4*3)+(3*7)+(2*2)+(1*9)=84
84 % 10 = 4
So 113137-29-4 is a valid CAS Registry Number.
InChI:InChI=1/C12H16ClNO2/c1-12(2,3)11(15)14-9-6-5-8(13)7-10(9)16-4/h5-7H,1-4H3,(H,14,15)
113137-29-4Relevant articles and documents
Discovery of atrop fixed alkoxy-aminobenzhydrol derivatives: Novel, highly potent and orally efficacious squalene synthase inhibitors
Ichikawa, Masanori,Yokomizo, Aki,Itoh, Masao,Haginoya, Noriyasu,Sugita, Kazuyuki,Usui, Hiroyuki,Terayama, Koji,Kanda, Akira
experimental part, p. 5207 - 5224 (2011/10/08)
We have recently reported the discovery of the new benzhydrol template, which has a highly potent inhibitory activity for squalene synthase, as typified by compound 1 (SSI IC50 = 0.85 nM). However, it was composed of a pair of easy rotatable at
Synthesis and biological activities of potential metabolites of the non-nucleoside reverse transcriptase inhibitor efavirenz
Markwalder, Jay A.,Christ, David D.,Mutlib, Abdul,Cordova, Beverly C.,Klabe, Ronald M.,Seitz, Steven P.
, p. 619 - 622 (2007/10/03)
Studies on the biotransformation of the clinically important non-nucleoside reverse transcriptase inhibitor efavirenz have shown that oxidation and secondary conjugation are important components of the processing of this molecule in vivo. We have synthesized metabolites of efavirenz to confirm their structure and to evaluate their activity as antivirals.
4,4-disubstitued-1,4-dihydro-2H-3,1-benzoxazin-2-ones useful as HIV reverse transcriptase inhibitors and intermediates and processes for making the same
-
, (2008/06/13)
The present invention relates to benzoxazinones of formula I: STR1 or stereoisomeric forms or mixtures, or pharmaceutically acceptable salt forms thereof, which are useful as inhibitors of HIV reverse transcriptase, and to pharmaceutical compositions and diagnostic kits comprising the same, methods of using the same for treating viral infection or as an assay standard or reagent, and intermediates and processes for making the same.