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(1S,3R,5R)-3-Formyl-8-aza-bicyclo[3.2.1]octane-8-carboxylic acid tert-butyl ester is a complex organic compound with a molecular formula of C14H23NO3. It is characterized by its bicyclic structure, featuring a formyl group and a carboxylic acid functional group, with a tert-butyl ester derivative. (1S,3R,5R)-3-Formyl-8-aza-bicyclo[3.2.1]octane-8-carboxylic acid tert-butyl ester is notable for its potential as a building block in the synthesis of biologically active molecules and pharmaceuticals, owing to its unique structure and reactivity. It also holds promise as a chiral ligand in asymmetric catalysis and as a precursor for developing new materials and organic compounds.

882041-98-7

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882041-98-7 Usage

Uses

Used in Pharmaceutical Synthesis:
(1S,3R,5R)-3-Formyl-8-aza-bicyclo[3.2.1]octane-8-carboxylic acid tert-butyl ester is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to contribute to the creation of biologically active molecules. Its unique structure allows for the development of new drugs with potential therapeutic applications.
Used in Asymmetric Catalysis:
In the field of catalysis, (1S,3R,5R)-3-Formyl-8-aza-bicyclo[3.2.1]octane-8-carboxylic acid tert-butyl ester is utilized as a chiral ligand. Its specific stereochemistry plays a crucial role in asymmetric catalysis, enabling the selective formation of enantiomerically pure compounds, which is vital for the production of high-quality pharmaceuticals and agrochemicals.
Used in Material Science:
(1S,3R,5R)-3-Formyl-8-aza-bicyclo[3.2.1]octane-8-carboxylic acid tert-butyl ester also serves as a precursor in material science, where it can be used to develop new materials and organic compounds. Its versatility in chemical reactions allows for the exploration of novel materials with improved properties for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 882041-98-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,2,0,4 and 1 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 882041-98:
(8*8)+(7*8)+(6*2)+(5*0)+(4*4)+(3*1)+(2*9)+(1*8)=177
177 % 10 = 7
So 882041-98-7 is a valid CAS Registry Number.

882041-98-7Downstream Products

882041-98-7Relevant academic research and scientific papers

1,3-Alkyl Transposition in Allylic Alcohols Enabled by Proton-Coupled Electron Transfer

Knowles, Robert R.,Seidler, Gesa,Zhao, Kuo

supporting information, p. 20190 - 20195 (2021/08/13)

A method is described for the isomerization of acyclic allylic alcohols into β-functionalized ketones via 1,3-alkyl transposition. This reaction proceeds via light-driven proton-coupled electron transfer (PCET) activation of the O?H bond in the allylic al

Substituted arylamides

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Page/Page column 50, (2010/10/20)

Substituted benzamide compounds are provided along with methods for the use of those compounds for treating cancer.

1- (2H-PYRAZOL -3-YL) -3YL) {4-`1- (BENZOYL) -PIPERIDIN-4-YLMETHYL!-PHENYL}-UREA DERIVATIVES AND RELATED COMPOUNDS AS INHBITORS OF P38 KINASE AND/OR TNF INHIBITORS FOR THE TREATMENT OF IMFLAMMATIONS

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Page 66, (2008/06/13)

The present invention provides compounds of Formula (I) Wherein ( ) is an optional ethylene bridge; R1 is alkyl, cycloalkyl, aryl or aryl substituted with one or more substituents selected from alkyl, alkoxy and amino, or R1 is pyridyl or pyridyl substitu

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