105619-13-4 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule of the compound.
Explanation
This describes the specific arrangement of atoms and functional groups in the molecule, which is crucial for understanding its chemical properties and reactivity.
Explanation
These functional groups are responsible for the compound's reactivity and its ability to undergo various chemical reactions.
Explanation
The compound's versatility and reactivity make it a valuable starting material for the production of a wide range of chemical products.
Explanation
The compound serves as a precursor in the synthesis of various dyes and pigments, which are used in various industries, such as textiles, plastics, and printing.
Explanation
The solubility of the compound in different solvents is an important factor to consider when designing chemical reactions and processes involving this compound.
Explanation
The compound's stability under typical conditions is essential for its use in various industrial applications, as it ensures that the compound will not decompose or react unexpectedly during processing.
Explanation
As with many chemicals, proper safety precautions should be taken when handling this compound to minimize the risk of exposure and potential health hazards.
Explanation
The compound's regulatory status can vary depending on the specific application and the country or region in which it is being used, which may impact its availability and use in certain industries.
Structure
Dimethyl ester derivative of 1,3(4H)-pyridinedicarboxylic acid with a methyl group at the carbon 4 position of the pyridine ring.
Functional Groups
Ester, Carboxylic Acid, Pyridine, and Methyl groups.
Applications
Building block in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals.
Intermediate
Used as an intermediate in the production of dyes and pigments.
Industrial Importance
Wide range of applications in the chemical and pharmaceutical industries.
Solubility
Soluble in organic solvents like ethanol, methanol, and acetone.
Stability
Stable under normal temperature and pressure conditions.
Safety
Handle with care due to potential irritant and toxic properties.
Regulatory Status
May be subject to specific regulations depending on the intended use and location.
Check Digit Verification of cas no
The CAS Registry Mumber 105619-13-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,6,1 and 9 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 105619-13:
(8*1)+(7*0)+(6*5)+(5*6)+(4*1)+(3*9)+(2*1)+(1*3)=104
104 % 10 = 4
So 105619-13-4 is a valid CAS Registry Number.
105619-13-4Relevant articles and documents
Synthesis, stability, and reactions of 10-Sn-5 tin ate complexes bearing four tin-carbon bonds
Yamamoto, Yohsuke,Sakaguchi, Akira,Ohashi, Noriko,Akiba, Kin-Ya
, p. 259 - 263 (1996)
The monocyclic organostannates (o-C6H4C(CF3)2O)SnR2(p-CH3C6H4)-Li+(2a-Li+(R = Me), 2b-Li- (R = tBu)) bearing four Sn-C bonds, which can be prepared from the reaction of tetracoordinate tin 3a (R = Me) and 3b (R = tBu) with p-CH3C6H4Li, were found to be thermally stable but were unstable to moisture giving 3 quantitatively upon aqueous workup. These ate complexes were inert toward some typical electrophiles such as p-methoxybenzaldehyde, but were reactive enough toward 1,3-bis(methoxycarbonyl)pyridinium chloride (8) to give corresponding alkylated(arylated) dihydropyridines (9). These are quite unique examples in the respect that organostannanes bearing four Sn-C bonds, which have been known to be reluctant to form compounds of higher coordination numbers, formed stable pentacoordinate ate complexes and showed unique reactivity which differed from that of lithium reagents such as p-CH3C6H4Li which could have formed upon dissociation from the ate complexes. The reaction of 3a with nBuLi gave complex mixtures after treatment with water indicating that the expected ate complexes (o-C6H4C(CF3)2O)SnMe2(nBu)-Ki-(2c-Li+) was thermally unstable and existed in an equilibrium with a ring-opened structure 5c.
