7531-49-9 Usage
Description
N,N'-Diacetyl-3,6,3',4',6'-penta-O-acetyl-1-chlorochitobioside, with the CAS number 7531-49-9, is a white solid compound that is useful in organic synthesis. It is a derivative of chitobioside, a disaccharide composed of two N-acetylglucosamine units, with additional acetyl and chloro groups attached to specific positions. This complex structure endows it with unique chemical properties that make it valuable in various applications.
Uses
Used in Organic Synthesis:
N,N'-Diacetyl-3,6,3',4',6'-penta-O-acetyl-1-chlorochitobioside is used as a key intermediate in organic synthesis for the development of new chemical compounds. Its unique structure allows for the creation of a wide range of derivatives with potential applications in various fields, such as pharmaceuticals, materials science, and agrochemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, N,N'-Diacetyl-3,6,3',4',6'-penta-O-acetyl-1-chlorochitobioside is used as a building block for the synthesis of novel drug candidates. Its structural features can be exploited to design and develop new therapeutic agents with improved pharmacological properties, such as enhanced bioavailability, selectivity, and potency.
Used in Materials Science:
In materials science, N,N'-Diacetyl-3,6,3',4',6'-penta-O-acetyl-1-chlorochitobioside can be utilized as a component in the development of advanced materials with specific properties. Its ability to form complexes with other molecules can be harnessed to create materials with unique characteristics, such as improved mechanical strength, thermal stability, or biocompatibility.
Used in Agrochemical Industry:
N,N'-Diacetyl-3,6,3',4',6'-penta-O-acetyl-1-chlorochitobioside can also find applications in the agrochemical industry, where it can be used as a starting material for the synthesis of new pesticides, herbicides, or fertilizers. Its unique chemical properties may contribute to the development of more effective and environmentally friendly agrochemical products.
Check Digit Verification of cas no
The CAS Registry Mumber 7531-49-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,3 and 1 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7531-49:
(6*7)+(5*5)+(4*3)+(3*1)+(2*4)+(1*9)=99
99 % 10 = 9
So 7531-49-9 is a valid CAS Registry Number.
7531-49-9Relevant articles and documents
NOVEL ANTI-INFLAMMATORY PRO-DRUGS
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Page/Page column 31-32, (2009/01/24)
The present invention relates to compounds according to formula (I): wherein R is selected from the group consisting of anti-inflammatory agents and pharmaceutically acceptable salts thereof, pharmaceutical compositions comprising compounds of formula (I) and the use of these pharmaceutical compositions for the treatment or prophylaxis of chronic inflammatory diseases, in particular those that are caused by chronically activated macrophages. The chronic inflammatory disease is in particular atherosclerosis, (rheumatoid) arthritis, an (auto)immune disease or sarcoidosis.
Probing the mechanism of a fungal glycosyltransferase essential for cell wall biosynthesis. UDP-Chitobiose is not a substrate for chitin synthase
Chang, Robert,Yeager, Adam R.,Finney, Nathaniel S.
, p. 39 - 41 (2007/10/03)
Chitin synthase is responsible for the biosynthesis of chitin, an essential component of the fungal cell wall. There is a long-standing question as to whether "processive" transferases such as chitin synthase operate in the same manner as non-processive transferases. The question arises from analysis of the polysaccharide structure - in chitin, for instance, each sugar residue is rotated ca. 180 deg relative to the preceding sugar in the chain. This requires that the enzyme account for the alternating "up/down" configuration during biosynthesis. An enzyme with a single active site, analogous to the non-processive transferases - would have to accommodate a distorted glycosidic linkage at every other synthetic step. An alternative proposal is that the enzyme might assemble the disaccharide donor, addressing the "up/down" conformational problem prior to polymer synthesis. We present compelling evidence that this latter hypothesis is incorrect.
Kombinierte chemoenzymatische Synthese von N-Glycoproteinbausteinen
Thiem, Joachim,Wiemann, Torsten
, p. 78 - 80 (2007/10/02)
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