100479-70-7 Usage
Explanation
Different sources of media describe the Explanation of 100479-70-7 differently. You can refer to the following data:
1. The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 12 carbon atoms, 14 hydrogen atoms, 2 nitrogen atoms, and 1 oxygen atom.
2. The compound is a solid, and its color is described as white to off-white, which means it can range from pure white to a slightly grayish or beige hue.
3. The compound dissolves well in organic solvents, such as alcohols, ethers, and hydrocarbons, which are typically used in chemical reactions and laboratory procedures.
4. The compound's structure consists of an imidazole ring, which is a heterocyclic ring with nitrogen and carbon atoms, and a phenyl group, which is a benzene ring with an attached alcohol functional group.
5. The compound is primarily used in the pharmaceutical industry for the development and production of drugs and medications.
6. As a reagent, the compound can participate in various chemical reactions, such as substitution, addition, or condensation, to form new compounds with different properties and applications.
Appearance
White to off-white powder
Solubility
Soluble in organic solvents
Chemical Structure
Contains an imidazole ring and a phenyl group
Applications
Building block in the synthesis of pharmaceuticals and other organic compounds
Industry
Pharmaceutical industry
Functionality
Can be used as a reagent in organic synthesis
Check Digit Verification of cas no
The CAS Registry Mumber 100479-70-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,4,7 and 9 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 100479-70:
(8*1)+(7*0)+(6*0)+(5*4)+(4*7)+(3*9)+(2*7)+(1*0)=97
97 % 10 = 7
So 100479-70-7 is a valid CAS Registry Number.
100479-70-7Relevant articles and documents
Mechanism-based enzymatic method for reliable determination of absolute configuration of chiral 1-substituted ethanols: Combination with NMR method
Ema, Tadashi,Yoshii, Masataka,Korenaga, Toshinobu,Sakai, Takashi
, p. 1223 - 1229 (2002)
It has been demonstrated that lipase is useful not only for kinetic resolution but also for the rapid determination of absolute configurations. We have previously proposed a mechanism represented by transition-state models to rationalize the enantioselect
RETRACTED ARTICLE: The Manganese(I)-Catalyzed Asymmetric Transfer Hydrogenation of Ketones: Disclosing the Macrocylic Privilege
Passera, Alessandro,Mezzetti, Antonio
supporting information, p. 187 - 191 (2019/12/11)
The bis(carbonyl) manganese(I) complex [Mn(CO)2(1)]Br (2) with a chiral (NH)2P2 macrocyclic ligand (1) catalyzes the asymmetric transfer hydrogenation of polar double bonds with 2-propanol as the hydrogen source. Ketones (43 substrates) are reduced to alcohols in high yields (up to >99 %) and with excellent enantioselectivities (90–99 % ee). A stereochemical model based on attractive CH–π interactions is proposed.
