75834-57-0 Usage
Uses
Used in Organic Synthesis:
(1-OXO-1,2,3,4-TETRAHYDRO-NAPHTHALEN-2-YL)-CARBAMIC ACID TERT-BUTYL ESTER is used as a synthetic intermediate for the preparation of various organic compounds. Its unique structure, including the naphthalene ring and carbamic acid moiety, allows it to participate in a range of chemical reactions, facilitating the synthesis of complex organic molecules.
Used in Chemical Research:
In the realm of chemical research, (1-OXO-1,2,3,4-TETRAHYDRO-NAPHTHALEN-2-YL)-CARBAMIC ACID TERT-BUTYL ESTER serves as a valuable compound for studying reaction mechanisms, exploring new synthetic pathways, and understanding the properties of related chemical entities. Its reactivity and structural features make it a useful tool for advancing knowledge in organic chemistry.
Used in Pharmaceutical Industry:
(1-OXO-1,2,3,4-TETRAHYDRO-NAPHTHALEN-2-YL)-CARBAMIC ACID TERT-BUTYL ESTER is used as a building block in the development of pharmaceutical agents. Its potential to be modified and incorporated into drug molecules makes it a candidate for the creation of new therapeutics, particularly those targeting specific biological pathways or receptors.
Used in Material Science:
In material science, (1-OXO-1,2,3,4-TETRAHYDRO-NAPHTHALEN-2-YL)-CARBAMIC ACID TERT-BUTYL ESTER may be utilized as a component in the design and synthesis of novel materials with unique properties. Its incorporation into polymers or other materials could lead to advancements in areas such as electronics, coatings, or specialty chemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 75834-57-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,8,3 and 4 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 75834-57:
(7*7)+(6*5)+(5*8)+(4*3)+(3*4)+(2*5)+(1*7)=160
160 % 10 = 0
So 75834-57-0 is a valid CAS Registry Number.
75834-57-0Relevant academic research and scientific papers
Experiments towards the Synthesis of the Ergot Alkaloids and Related Structures. Part 2. New Alkylations on α-Carbon and Nitrogen in α-Amidoketones.
Bowman, Ralph E.
, p. 2126 - 2133 (2007/10/02)
The alkylation of a number of α-amidoketones in the 3,4-dihydro-naphthalen-1(2H)-one and acenaphthen-5(2aH)-one series, involving treatment with sodium hydride (1 or 2 mol equiv.) in dimethylformamide solution and subsequent reaction with alkyl halides, h
