6302-91-6 Usage
Physical state
Colorless liquid This compound is a liquid that appears colorless, meaning it does not have any visible color.
Odor
Strong, unpleasant The compound has a strong and unpleasant odor, which can be detected at low concentrations.
Uses
Intermediate in synthesis 2-(4-chlorophenyl)-2-methyl-1,3-dithiolane is used as an intermediate in the production of pharmaceuticals and agricultural chemicals, meaning it is a key component in the synthesis of other compounds.
Flavoring agent
Food industry This compound is also used as a flavoring agent in the food industry, adding taste and aroma to various food products.
Potential applications
Insecticidal and antifungal properties 2-(4-chlorophenyl)-2-methyl-1,3-dithiolane has been studied for its potential to act as an insecticide and antifungal agent, which could be useful in controlling pests and fungi in various settings.
Safety concerns
Harmful if ingested, inhaled, or in contact with skin It is important to handle this compound with care, as it can cause harm if it is ingested, inhaled, or comes into contact with the skin. Proper safety measures should be taken when working with this chemical.
Check Digit Verification of cas no
The CAS Registry Mumber 6302-91-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,0 and 2 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6302-91:
(6*6)+(5*3)+(4*0)+(3*2)+(2*9)+(1*1)=76
76 % 10 = 6
So 6302-91-6 is a valid CAS Registry Number.
6302-91-6Relevant articles and documents
PhIO-Mediated oxidative dethioacetalization/dethioketalization under water-free conditions
Du, Yunfei,Ouyang, Yaxin,Wang, Xi,Wang, Xiaofan,Yu, Zhenyang,Zhao, Bingyue,Zhao, Kang
, p. 48 - 65 (2021/06/16)
Treatment of thioacetals and thioketals with iodosobenzene in anhydrous DCM conveniently afforded the corresponding carbonyl compounds in high yields under water-free conditions. The mechanistic studies indicate that this dethioacetalization/dethioketalization process does not need water and the oxygen of the carbonyl products comes from the hypervalent iodine reagent.
Poly(N-bromobenzene-1,3-disulfonamide) and N,N,N′,N′- tetrabromobenzene-1,3-disulfonamide as a mild and efficient catalyst for chemoselective thioacetalization of carbonyl functions and transthioacetalization reactions
Veisi, Hojat,Ghorbani-Vaghei, Ramin,Dadamahaleh, Somayeh Akbari
experimental part, p. 699 - 705 (2011/07/31)
Poly(N-bromobenzene-1,3-disulfonamide) and N,N,N′,N′- tetrabromobenzene-1,3-disulfonamide are effective catalysts for chemoselective dithioacetalization of aldehydes in the presence of ketones under neutral conditions.
An efficient, continuous flow technique for the chemoselective synthesis of thioacetals
Wiles, Charlotte,Watts, Paul,Haswell, Stephen J.
, p. 7362 - 7365 (2008/03/13)
By optimizing a reagent's residence time within a packed-bed reactor, it is possible to overcome selectivity issues frequently encountered in stirred reaction vessels. This important feature is demonstrated for the chemoselective protection of 4-acetylben
