171808-04-1 Usage
Description
METHYL 6'-DESMETHYL-4'-TOSYLMYCOPHENOLATE, with the CAS number 171808-04-1, is a compound that is characterized by its slight yellow foam appearance. It is primarily utilized in the field of organic synthesis, where it serves as a valuable component for creating various chemical structures and compounds.
Uses
Used in Organic Synthesis:
METHYL 6'-DESMETHYL-4'-TOSYLMYCOPHENOLATE is used as a synthetic building block for the creation of a wide range of organic compounds. Its unique chemical structure allows it to be a versatile and valuable component in the synthesis of various molecules, contributing to the development of new materials and pharmaceuticals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, METHYL 6'-DESMETHYL-4'-TOSYLMYCOPHENOLATE is used as a key intermediate in the synthesis of various drugs. Its chemical properties make it suitable for the development of new medications, potentially leading to the discovery of novel therapeutic agents.
Used in Chemical Research:
METHYL 6'-DESMETHYL-4'-TOSYLMYCOPHENOLATE is also employed in chemical research, where it can be used to study the properties and behavior of different compounds. Its slight yellow foam appearance and unique structure make it an interesting subject for researchers to explore and understand the underlying principles of chemical reactions and interactions.
Check Digit Verification of cas no
The CAS Registry Mumber 171808-04-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,1,8,0 and 8 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 171808-04:
(8*1)+(7*7)+(6*1)+(5*8)+(4*0)+(3*8)+(2*0)+(1*4)=131
131 % 10 = 1
So 171808-04-1 is a valid CAS Registry Number.
171808-04-1Relevant articles and documents
Mycophenolic acid as a latent agonist of PPARγ
Ubukata, Makoto,Takamori, Hitomi,Ohashi, Misaki,Mitsuhashi, Shinya,Yamashita, Kaoru,Asada, Tomohisa,Nakajima, Noriyuki,Matsuura, Nobuyasu,Tsuruga, Mie,Taki, Keiko,Magae, Junji
, p. 4767 - 4770 (2008/02/11)
Mycophenolic acid (MPA), known as an inhibitor of inosine monophosphate dehydrogenase (IMPDH), was found to inhibit the differentiation of 3T3-L1 pre-adipocytes into mature adipocytes. Although the effect of MPA was attributed to inhibition of IMPDH, we u
Structure-activity relationships for inhibition of inosine monophosphate dehydrogenase by nuclear variants of mycophenolic acid
Nelson, Peter H.,Carr, Stephen F.,Devens, Bruce H.,Eugui, Elsie M.,Franco, Fidencio,Gonzalez, Carlos,Hawley, Ronald C.,Loughhead, David G.,Milan, David J.,Papp, Eva,Patterson, John W.,Rouhafza, Sussan,Sjogren, Eric B.,Smith, David B.,Stephenson, Rebecca A.,Talamas, Francisco X.,Waltos, Ann-Marie,Weikert, Robert J.,Wu, John C.
, p. 4181 - 4196 (2007/10/03)
Structure-activity relationships in the region of the phthalide ring of the inosine monophosphate dehydrogenase inhibitor mycophenolic acid have been explored. Replacement of the lactone ring with other cyclic moieties resulted in loss of potency, especia
