1675248-18-6 Usage
Description
1-Piperidinepropanoic acid, 4-methyl-3-(methyl-7H-pyrrolo[2,3-d]pyrimidin-4-ylamino)-β-oxo-, ethyl ester, (3R,4R)is a complex organic compound with a unique molecular structure. It is characterized by its piperidinepropanoic acid backbone, which is substituted with a methyl group and a pyrrolo[2,3-d]pyrimidin-4-ylamino moiety. The molecule also features a β-oxo group and an ethyl ester functional group, with the stereochemistry being (3R,4R)-. 1-Piperidinepropanoic acid, 4-methyl-3-(methyl-7H-pyrrolo[2,3-d]pyrimidin-4-ylamino)-β-oxo-, ethyl ester, (3R,4R)is likely to have specific applications in various industries due to its unique structure and properties.
Uses
Used in Pharmaceutical Industry:
1-Piperidinepropanoic acid, 4-methyl-3-(methyl-7H-pyrrolo[2,3-d]pyrimidin-4-ylamino)-β-oxo-, ethyl ester, (3R,4R)is used as an active pharmaceutical ingredient (API) for the development of novel therapeutic agents. Its unique molecular structure and stereochemistry make it a promising candidate for targeting specific biological pathways and receptors, potentially leading to the treatment of various diseases and conditions.
Used in Chemical Research:
In the field of chemical research, 1-Piperidinepropanoic acid, 4-methyl-3-(methyl-7H-pyrrolo[2,3-d]pyrimidin-4-ylamino)-β-oxo-, ethyl ester, (3R,4R)can be used as a starting material or intermediate for the synthesis of more complex molecules with potential applications in various industries. Its unique structure and functional groups make it an interesting target for further modification and optimization.
Used in Drug Synthesis:
1-Piperidinepropanoic acid, 4-methyl-3-(methyl-7H-pyrrolo[2,3-d]pyrimidin-4-ylamino)-β-oxo-, ethyl ester, (3R,4R)is used as a key intermediate in the synthesis of various drug candidates. Its unique structure and functional groups can be exploited to design and develop new drugs with improved pharmacological properties, such as increased potency, selectivity, and reduced side effects.
Used in Impurity Profiling:
As an impurity compound of Tofacitinib (C781351), a Janus kinase inhibitor used for the treatment of rheumatoid arthritis, 1-Piperidinepropanoic acid, 4-methyl-3-(methyl-7H-pyrrolo[2,3-d]pyrimidin-4-ylamino)-β-oxo-, ethyl ester, (3R,4R)is used in the quality control and impurity profiling of Tofacitinib. Understanding and controlling the presence of this impurity is crucial for ensuring the safety, efficacy, and quality of the final drug product.
Check Digit Verification of cas no
The CAS Registry Mumber 1675248-18-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,7,5,2,4 and 8 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1675248-18:
(9*1)+(8*6)+(7*7)+(6*5)+(5*2)+(4*4)+(3*8)+(2*1)+(1*8)=196
196 % 10 = 6
So 1675248-18-6 is a valid CAS Registry Number.
1675248-18-6Relevant articles and documents
Preparation method oftofacitinib impurity I
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Paragraph 0012; 0035-0036; 0038-0039; 0041-0042; 0044; ...., (2021/10/27)
The invention provides a preparation method of a tofacitinib impurity I. According to the method, monosubstituted sylvite is used for reaction, a high-purity product can be obtained by directly hydrolyzing an intermediate without purification operation, and a sylvite reaction system is stable; and DMTMM is used as a condensing agent, the reaction operation is simple, the reaction condition is mild, compared with a common condensing agent, the reaction system has few side reactions, corresponding impurity byproducts are hardly generated, the reaction efficiency is high, the yield is high, and the method is suitable for batch production.
A supporting france for cloth related substance preparation method and application of (by machine translation)
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Paragraph 0020-0022; 0028-0029, (2019/07/04)
The invention supporting france for cloth on the preparation method of the substance and application, provides a support france for cloth material type III shown in the preparation of the compounds of the method, the method is simple in operation, the product has high purity, can quickly obtaining high purity of the material holds the law for the cloth of the reference substance, is beneficial for the quality of fabrics Fischer research, impurity control, thereby improving the Tropsch process for the cloth quality control level. Type III. (by machine translation)
