174590-62-6 Usage
Explanation
This is the full name of the compound, which describes its structure and stereochemistry.
Explanation
The compound is a type of alcohol that contains two rings and has an ester group derived from benzoic acid.
Explanation
The compound has a specific arrangement of atoms in space, with the hydroxyl group (-OH) on the 3rd carbon in the R configuration.
Explanation
The compound is used in these fields due to its unique structure and potential for the synthesis of medicinally important compounds.
Explanation
The compound serves as a building block or intermediate in the creation of other pharmaceutical compounds.
Explanation
Due to its structural and functional properties, the compound may be useful in the development and production of new drugs.
Explanation
The compound may have specific safety concerns and potential hazards associated with its use, so it is important to follow proper handling and safety protocols.
Explanation
The material does not provide specific information about the hazards associated with this compound, but it is important to be aware of potential risks when working with any chemical compound.
Classification
Bicyclic alcohol with a benzoate ester group
Stereochemistry
(3R)configuration
Field of Application
Organic chemistry and pharmaceuticals
Synthesis
Used in the synthesis of various medicinally important compounds
Potential Applications
Drug development and manufacturing
Safety Considerations
Handle and use with caution
Potential Hazards
Not specified in the material provided
Check Digit Verification of cas no
The CAS Registry Mumber 174590-62-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,4,5,9 and 0 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 174590-62:
(8*1)+(7*7)+(6*4)+(5*5)+(4*9)+(3*0)+(2*6)+(1*2)=156
156 % 10 = 6
So 174590-62-6 is a valid CAS Registry Number.
174590-62-6Relevant articles and documents
Simple one-pot process for the bioresolution of tertiary amino ester protic ionic liquids using subtilisin
Brossat, Maude,Moody, Thomas S.,Taylor, Stephen J.C.,Wiffen, Jonathan W.
experimental part, p. 2112 - 2116 (2010/02/28)
An efficient hydrolase-catalyzed bioresolution of tertiary amino ester protic ionic liquids has been demonstrated. Protic ionic liquids have been prepared in one step from the corresponding tertiary amino alcohols by treatment with butyric anhydride. Afte
