52894-99-2 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule of the compound.
Explanation
This describes the physical appearance of the compound in its solid state.
Explanation
The compound has a range of uses in different industries, making it versatile.
Explanation
The compound contributes to the scent and flavor of various products, such as perfumes and other scented items.
Explanation
The compound serves as a starting material or intermediate in the production of pharmaceuticals and other organic compounds.
Explanation
The compound may pose health risks if not handled with care, emphasizing the importance of proper safety measures during its use.
Appearance
Yellow to orange solid
Industrial applications
Various
Use as a cross-linking agent
Polymer and resin manufacturing
Use in fragrance and flavoring
Perfumes and scented products
Utilization in synthesis
Pharmaceuticals and organic compounds
Health risks
Potential hazards if mishandled or improperly used
Check Digit Verification of cas no
The CAS Registry Mumber 52894-99-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,8,9 and 4 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 52894-99:
(7*5)+(6*2)+(5*8)+(4*9)+(3*4)+(2*9)+(1*9)=162
162 % 10 = 2
So 52894-99-2 is a valid CAS Registry Number.
52894-99-2Relevant articles and documents
Palladium-Catalyzed C-S Bond Cleavage with Allenoates: Synthesis of Tetrasubstituted 2-Alkenylfuran Derivatives
Wang, Quannan,Liu, Zhuqing,Lou, Jiang,Yu, Zhengkun
supporting information, p. 6007 - 6011 (2018/10/09)
Palladium-catalyzed C-S cleavage of tetrasubstituted internal alkene α-oxo ketene dithioacetals was realized with allenoates as the coupling partners, efficiently affording tetrasubstituted 2-alkenylfuran derivatives with excellent regioselectivity under mild conditions. Allenoates acted as C1 synthons in the desulfurative [4 + 1] annulation.
A convenient synthesis of 2,3,4,5-functionalised thieno[2,3-b]thiophenes
Sommen, Geoffroy,Comel, Alain,Kirsch, Gilbert
, p. 735 - 741 (2007/10/03)
A two steps simple synthesis of 2,3,4,5-functionalised thieno[2,3-b]thiophenes 2-6 from ketene dimethylthioacetals is described.
A convenient one-pot synthesis of ketene dithioacetals
Villemin,Alloum
, p. 301 - 303 (2007/10/02)
An easy synthesis of ketene dithioacetals 2 and 3 by the condensation of carbon disulfide and active methylene compounds 1 with subsequent alkylation in the presence of potassium fluoride is described.
