5406-38-2 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule of the compound.
Explanation
It is a derivative of dioxane, which means it is structurally related to dioxane but has undergone a chemical modification.
Explanation
The compound contains a chlorine atom that is part of a phenyl ring, which is a six-carbon ring with alternating single and double bonds.
Explanation
It is used as an intermediate in the production of various pharmaceuticals, pesticides, and other organic chemicals due to its chemical reactivity.
Explanation
It is used as a solvent in various industrial processes, taking advantage of its ability to dissolve other substances.
Explanation
Studies have shown that 1,3-Dioxane, 2-(2-chlorophenyl)-(9CI) may have carcinogenic properties, meaning it could potentially cause cancer.
Explanation
The compound has been found to have toxic effects on human health and the environment, which is why its use and disposal should be carefully managed.
Explanation
Proper handling, storage, and disposal methods are essential to minimize the risks associated with the compound's potential carcinogenic and toxic effects.
Derivative of Dioxane
Yes
Chlorine Atom
Attached to a phenyl ring
Common Uses
Pharmaceutical synthesis, pesticide synthesis, and other organic chemicals
Industrial Application
Solvent
Potential Carcinogenic Effects
Yes
Toxic Effects
Yes
Environmental and Health Risks
High
Disposal and Management
Careful handling required
Check Digit Verification of cas no
The CAS Registry Mumber 5406-38-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,0 and 6 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5406-38:
(6*5)+(5*4)+(4*0)+(3*6)+(2*3)+(1*8)=82
82 % 10 = 2
So 5406-38-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H11ClO2/c11-9-5-2-1-4-8(9)10-12-6-3-7-13-10/h1-2,4-5,10H,3,6-7H2
5406-38-2Relevant articles and documents
Practical acetalization and transacetalization of carbonyl compounds catalyzed by recyclable PVP-I
Cao, Fu-Rong,Lu, Guangying,Ren, Jiangmeng,Wang, Di,Zeng, Bu-Bing
, (2021/06/21)
A novel PVP-I catalyzed acetalizations/transacetalizations of carbonyl compounds has been developed processing with a mild and easy handling fashion. Different types of Acyclic and cyclic acetals were prepared from carbonyl compounds or their acetals successfully. Further applications of newly developed catalytic combination were testified. This protocol featured with simplicity of operation, mild reaction condition, short reaction time, recyclable of catalyst and broad substrates scope with excellent yields.
Acetalization of carbonyl compounds catalyzed by bismuth triflate under solvent-free conditions
Aliyan, Hamid,Fazaeli, Razieh,Massah, Ahmad Reza,Momeni, Ahmad Reza,Naghash, Hamid Javaherian,Moeinifard, Behzad
experimental part, p. 873 - 876 (2012/04/05)
Carbonyl compounds were converted to the corresponding 1,3-dioxolanes and 1,3-dioxanes with ethylene glycol and 1,3-propandiol in the presence of bismuth triflate under solvent-free conditions. In addition, high chemoselective protection of aldehydes in the presence of ketones has been achieved.
2,4,4,6-Tetrabromo-2,5-cyclohexadienone (TABCO) as a versatile, efficient, and chemoselective catalyst for the acetalization and transacetalization of carbonyl compounds, the preparation of acetonides from epoxides and acylals (1,1-diacetates) from aldehydes
Firouzabadi, Habib,Iranpoor, Nasser,Shaterian, Hamid Reza
, p. 2195 - 2205 (2007/10/03)
The efficient and chemoselective preparation of acetals and ketals from carbonyl compounds, transacetalization reactions, the conversion of epoxides to acetonides, and the preparation of acylals from aldehydes in the presence of catalytic amounts of 2,4,4,6-tetrabromo-2,5-cyclohexadienone (TABCO) are described.
