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TERT-BUTYL 1,3-DIOXO-2,8-DIAZASPIRO[4.5]DECANE-8-CARBOXYLATE is a spirocyclic chemical compound with the molecular formula C14H23N3O5. It features a diazabicycloalkane skeleton and is derived from tert-butyl carboxylic acid. TERT-BUTYL 1,3-DIOXO-2,8-DIAZASPIRO[4.5]DECANE-8-CARBOXYLATE has potential applications in the pharmaceutical and agrochemical industries due to its biological activities, such as anti-inflammatory and insecticidal properties. However, its precise properties and potential hazards are still under investigation, and caution is advised in handling TERT-BUTYL 1,3-DIOXO-2,8-DIAZASPIRO[4.5]DECANE-8-CARBOXYLATE.

752234-60-9

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752234-60-9 Usage

Uses

Used in Pharmaceutical Industry:
TERT-BUTYL 1,3-DIOXO-2,8-DIAZASPIRO[4.5]DECANE-8-CARBOXYLATE is used as a pharmaceutical agent for its anti-inflammatory properties. It may be utilized in the development of drugs targeting inflammation-related conditions, offering potential therapeutic benefits.
Used in Agrochemical Industry:
In the agrochemical industry, TERT-BUTYL 1,3-DIOXO-2,8-DIAZASPIRO[4.5]DECANE-8-CARBOXYLATE is used as an insecticidal agent. Its insecticidal properties make it a candidate for the development of pesticides to control pests in agriculture, thereby protecting crops and increasing yield.

Check Digit Verification of cas no

The CAS Registry Mumber 752234-60-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,5,2,2,3 and 4 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 752234-60:
(8*7)+(7*5)+(6*2)+(5*2)+(4*3)+(3*4)+(2*6)+(1*0)=149
149 % 10 = 9
So 752234-60-9 is a valid CAS Registry Number.
InChI:InChI=1/C13H20N2O4/c1-12(2,3)19-11(18)15-6-4-13(5-7-15)8-9(16)14-10(13)17/h4-8H2,1-3H3,(H,14,16,17)

752234-60-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl 1,3-dioxo-2,8-diazaspiro[4.5]decane-8-carboxylate

1.2 Other means of identification

Product number -
Other names 2,5-DIMETHYLTHIOPHENE-3-BORONIC ACID

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:752234-60-9 SDS

752234-60-9Relevant academic research and scientific papers

Effect of cathepsin K inhibitors on bone resorption

Teno, Naoki,Masuya, Keiichi,Ehara, Takeru,Kosaka, Takatoshi,Miyake, Takahiro,Irie, Osamu,Hitomi, Yuko,Matsuura, Naoko,Umemura, Ichiro,Iwasaki, Genji,Fukaya, Hiroaki,Toriyama, Kazuhiro,Uchiyama, Noriko,Nonomura, Kazuhiko,Sugiyama, Ikuo,Kometani, Motohiko

experimental part, p. 5459 - 5462 (2009/07/09)

On the basis of the pyrrolopyrimidine core structure that was previously discovered, cathepsin K inhibitors having a spiro amine at the P3 have been explored to enhance the target, bone marrow, tissue distribution. Several spiro structures were identified with improved distribution toward bone marrow. The representative inhibitor 7 of this series revealed in vivo reduction in C-terminal telopeptide of type I collagen in rats and monkeys.

SPIRO-SUBSTITUTED PYRROLOPYRIMIDINES

-

Page 19; 34-35, (2008/06/13)

The invention provides compounds of formula (I) or a pharmaceutically acceptable salt or ester thereof formula (I) wherein the symbols have the meaning as defined in the description. Said compounds are inhibitors of cathepsin K and/or cathepsin S and are useful for the treatment of diseases and medical conditions in which cathepsin K and/or cathepsin S is implicated, e.g. various disorders including neuropathic pain, inflammation, rheumatoid arthritis, osteoarthritis, osteoporosis, multiple sclerosis and tumours.

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