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Tert-butyl 1-oxo-2,7-diazaspiro[4.5]decane-7-carboxylate is a complex chemical compound characterized by a unique spiro ring system, a diaza bridge, and a decane backbone. It incorporates a tert-butyl group, an oxo group, and a carboxylate group, which contribute to its diverse functional groups and potential biological activities. tert-butyl 1-oxo-2,7-diazaspiro[4.5]decane-7-carboxylate is of interest to chemists and researchers for its intriguing molecular architecture and possible applications in organic synthesis and pharmaceutical research.

923009-50-1

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923009-50-1 Usage

Uses

Used in Organic Synthesis:
Tert-butyl 1-oxo-2,7-diazaspiro[4.5]decane-7-carboxylate is used as a building block in organic synthesis for its versatile functional groups that can be further modified or utilized in the construction of more complex molecules.
Used in Pharmaceutical Research:
In the pharmaceutical industry, tert-butyl 1-oxo-2,7-diazaspiro[4.5]decane-7-carboxylate is used as a starting material or intermediate in the development of new drugs. Its unique structure and functional groups may offer novel biological activities, making it a promising candidate for drug discovery and design.
Used in Drug Discovery:
Tert-butyl 1-oxo-2,7-diazaspiro[4.5]decane-7-carboxylate is employed as a scaffold in drug discovery for its potential to be optimized and modified to target specific biological pathways or receptors, leading to the development of innovative therapeutic agents.
Used in Chemical Research:
In the field of chemical research, tert-butyl 1-oxo-2,7-diazaspiro[4.5]decane-7-carboxylate is used as a subject of study to explore its reactivity, stability, and interactions with other molecules, contributing to the understanding of complex chemical systems and the development of new synthetic strategies.

Check Digit Verification of cas no

The CAS Registry Mumber 923009-50-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,3,0,0 and 9 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 923009-50:
(8*9)+(7*2)+(6*3)+(5*0)+(4*0)+(3*9)+(2*5)+(1*0)=141
141 % 10 = 1
So 923009-50-1 is a valid CAS Registry Number.
InChI:InChI=1/C15H26N2O3/c1-5-16-10-8-15(12(16)18)7-6-9-17(11-15)13(19)20-14(2,3)4/h5-11H2,1-4H3

923009-50-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-Butyl 1-oxo-2,7-diazaspiro[4.5]decane-7-carboxylate

1.2 Other means of identification

Product number -
Other names tert-butyl 1-oxo-2,9-diazaspiro[4.5]decane-9-carboxylate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:923009-50-1 SDS

923009-50-1Downstream Products

923009-50-1Relevant academic research and scientific papers

2-[BIS(4-FLUOROPHENYL)METHYL]-2,7-DIAZASPIRO[4.5]DECAN-10-ONE DERIVATIVES AND RELATED COMPOUNDS AS INHIBITORS OF THE HUMAN DOPAMINE-ACTIVE-TRANSPORTER (DAT) PROTEIN FOR THE TREATMENT OF E.G. ATTENTION DEFICIT DISORDER (ADD)

-

Page/Page column 84, (2016/04/09)

The present invention provides compounds of formula (I) and in particular 2-[bis(4-fluorophenyl)methyl]-2,7- diazaspiro[4.5]decan-10-one derivatives and related compounds as inhibitors of human dopamine-active-transporter (DAT) protein for the treatment of sexual dysfunction, affective disorders, anxiety, depression, chronic fatigue, Tourette syndrome, Angelman syndrome, attention deficit disorder (ADD), attention deficit hyperactivity disorder (ADHD), obesity, pain, obsessive-compulsive disorder, movement disorders, CNS disorders, sleep disorders, narcolepsy, conduct disorder, substance abuse (including smoking cessation), eating disorders, and impulse control disorders.

Design, synthesis, and structure-activity relationships of spirolactones bearing 2-ureidobenzothiophene as acetyl-CoA carboxylases inhibitors

Yamashita, Tohru,Kamata, Makoto,Endo, Satoshi,Yamamoto, Mitsuo,Kakegawa, Keiko,Watanabe, Hiroyuki,Miwa, Katsuhiko,Yamano, Toru,Funata, Masaaki,Sakamoto, Jyun-Ichi,Tani, Akiyoshi,Mol, Clifford D.,Zou, Hua,Dougan, Douglas R.,Sang, BiChing,Snell, Gyorgy,Fukatsu, Kohji

, p. 6314 - 6318 (2011/11/29)

The co-crystal structure of the human acetyl-coenzyme A 2 (ACC2) carboxyl transferase domain and the reported compound CP-640186 (1b) suggested that two carbonyl groups are essential for potent ACC2 inhibition. By focusing on enhancing the interactions between the two carbonyl groups and the amino acid residues Gly2162 and Glu2230, we used ligand- and structure-based drug design to discover spirolactones bearing a 2-ureidobenzothiophene moiety

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