251645-83-7 Usage
Description
(1S,E)-(-)-Camphorquinone 3-oxime is a chemical compound characterized by its molecular formula C10H13NO2. It is known for its camphor-like odor and typically appears as a yellowish to brown crystalline solid at room temperature. (1S,E)-(-)-Camphorquinone 3-oxime plays a significant role in the field of organic chemistry, particularly as a reagent in the synthesis of various organic compounds.
Uses
Used in Organic Chemistry:
(1S,E)-(-)-Camphorquinone 3-oxime is used as a reagent in organic chemistry for the synthesis of different organic compounds, contributing to the development of new chemical entities and materials.
Used in Dental Applications:
In the dental industry, (1S,E)-(-)-Camphorquinone 3-oxime is used as a photoinitiator for the polymerization of dental resins. Its application facilitates the curing process, ensuring the proper hardening and setting of dental materials to achieve optimal dental restorations.
Used in Antimicrobial Development:
(1S,E)-(-)-Camphorquinone 3-oxime has been studied for its potential use in the development of antimicrobial agents. Its properties are being explored to create new compounds that can effectively combat microbial infections.
Used as a Chiral Auxiliary in Organic Synthesis:
Furthermore, (1S,E)-(-)-Camphorquinone 3-oxime serves as a chiral auxiliary in organic synthesis. This application is crucial for the production of enantiomerically pure compounds, which are essential in various pharmaceutical and chemical industries.
Check Digit Verification of cas no
The CAS Registry Mumber 251645-83-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,1,6,4 and 5 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 251645-83:
(8*2)+(7*5)+(6*1)+(5*6)+(4*4)+(3*5)+(2*8)+(1*3)=137
137 % 10 = 7
So 251645-83-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H15NO2/c1-11-7-3-5-8(10(12)13-2)9(11)6-4-7/h5,7,9H,3-4,6H2,1-2H3
251645-83-7Relevant articles and documents
Chiral thiourea derivatives as organocatalyts in the enantioselective Morita- Baylis-Hillman reactions
Aydin, A. Ebru
, (2020/08/28)
Novel chiral bifunctional thiourea derivatives have been synthesised and successfully applied to the intermolecular Morita-Baylis-Hillman (MBH) reaction of an aromatic aldehyde with methyl vinyl ketone (MVK) and to the intramolecular MBH reaction of ω-for
(2S)-(–)-3-exo-(morpholino)isoborneol [(–)-MIB] ([1R-(exo,exo)]-1,7,7-Trimethyl-3-morpholin-4-yl-bicyclo[2.2.1] heptan-2-ol)
Chen, Young K.,Jeon, Sang-Jin,Walsh, Patrick J.,Nugent, William A.,Kendall, Christopher,Wipf, Peter
, p. 87 - 92 (2017/09/08)
-
