106622-89-3 Usage
Explanation
Different sources of media describe the Explanation of 106622-89-3 differently. You can refer to the following data:
1. The molecular formula represents the number of atoms of each element present in a molecule of the compound.
2. The physical state and color of the compound, which is a colorless liquid in this case.
3. The characteristic smell of the compound, which is described as fruity.
4. The primary applications of the compound in the chemical industry, which include the production of various drugs and organic compounds.
5. The compound serves as a fundamental component in the creation of different pharmaceuticals.
6. The compound can also be found in the fragrance and flavoring industries, contributing to the scents and tastes of various products.
7. The compound acts as an intermediate in the synthesis of a wide range of organic compounds, highlighting its versatility.
8. The compound is recognized for its ability to maintain its structure and properties during chemical reactions.
9. The compound is also known for its ability to readily participate in chemical reactions, making it a valuable component in various synthesis processes.
Appearance
Colorless liquid
Odor
Fruity
Uses
Synthesis of pharmaceuticals and organic compounds
Building Block
Production of various drugs
Presence in
Perfumes and flavorings
Intermediate
Synthesis of various organic compounds
Stability
Known for its stability in chemical reactions
Reactivity
Known for its reactivity in chemical reactions
Check Digit Verification of cas no
The CAS Registry Mumber 106622-89-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,6,2 and 2 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 106622-89:
(8*1)+(7*0)+(6*6)+(5*6)+(4*2)+(3*2)+(2*8)+(1*9)=113
113 % 10 = 3
So 106622-89-3 is a valid CAS Registry Number.
106622-89-3Relevant articles and documents
Synthesis of pluraflavin A "aglycone"
Wright, Benjamin J. D.,Hartung, John,Peng, Feng,Van De Water, Ryan,Liu, Haibo,Tan, Quen-Hui,Chou, Ting-Chao,Danishefsky, Samuel J.
supporting information; experimental part, p. 16786 - 16790 (2009/04/14)
The "aglycone" of pluraflavin A (2) has been synthesized. The key features of this synthesis include a 1,3-dipolar cycloaddition between a nitrile oxide (cf. 14) and an olefin (22) to yield an isoxazoline followed by subsequent conversion into the γ-pyrone of pluraflavin A. The epoxide moiety linked to the pyrone is installed prior to Diels-Alder installation of the D ring, which allows access to a number of potentially active cytotoxic intermediates en route to the final compound. The preliminary in vitro results of two such compounds are also included with the racemic title compound exhibiting cytotoxicity in the nanomolar range.
Stereochemistry and Synthetic Applications of the Products of Yeast Reduction of 3-Hydroxy-3-methyl-5-phenylpent-4-en-2-one
Fronza, Giovanni,Fuganti, Claudio,Pedrocchi-Fantoni, Giuseppe,Servi, Stefano
, p. 1141 - 1144 (2007/10/02)
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