6823-42-3 Usage
Explanation
Different sources of media describe the Explanation of 6823-42-3 differently. You can refer to the following data:
1. This is an alternative name for 1,3-Benzodioxole, 2-methoxy-, which is used to describe its structure and properties.
2. The compound is in a liquid state at room temperature and is colorless, meaning it does not have any visible color.
3. The compound has a pleasant scent that is described as slightly sweet and floral, making it suitable for use in perfumes and flavorings.
4. Due to its pleasant scent, 1,3-Benzodioxole, 2-methoxyis used in the production of perfumes and flavorings. Additionally, it is utilized in the creation of pharmaceuticals and agrochemicals, indicating its versatility in various industries.
5. As a flammable substance, 1,3-Benzodioxole, 2-methoxyposes a risk of ignition and should be handled and stored with care to prevent accidents or fires.
6. Due to its flammable nature, it is crucial to follow safety guidelines when handling and storing 1,3-Benzodioxole, 2-methoxyto minimize the risk of accidents or fires.
Physical state
Colorless liquid
Odor
Slightly sweet, floral
Applications
Perfumes, flavorings, pharmaceuticals, and agrochemicals
Flammability
Flammable
Safety precautions
Handle and store with care
Check Digit Verification of cas no
The CAS Registry Mumber 6823-42-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,8,2 and 3 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6823-42:
(6*6)+(5*8)+(4*2)+(3*3)+(2*4)+(1*2)=103
103 % 10 = 3
So 6823-42-3 is a valid CAS Registry Number.
6823-42-3Relevant articles and documents
Decatungstate-Mediated C(sp3)–H Heteroarylation via Radical-Polar Crossover in Batch and Flow
Capaldo, Luca,Frederick, Michael O.,García-Losada, Pablo,Laudadio, Gabriele,Mateos, Carlos,No?l, Timothy,Nu?o, Manuel,Nyuchev, Alexander V.,Rincón, Juan A.,Wan, Ting
supporting information, p. 17893 - 17897 (2021/07/14)
Photocatalytic hydrogen atom transfer is a very powerful strategy for the regioselective C(sp3)–H functionalization of organic molecules. Herein, we report on the unprecedented combination of decatungstate hydrogen atom transfer photocatalysis with the oxidative radical–polar crossover concept to access the direct net-oxidative C(sp3)–H heteroarylation. The present methodology demonstrates a high functional group tolerance (40 examples) and is scalable when using continuous-flow reactor technology. The developed protocol is also amenable to the late-stage functionalization of biologically relevant molecules such as stanozolol, (?)-ambroxide, podophyllotoxin, and dideoxyribose.
