745783-80-6 Usage
Description
(R)-(-)-1-INDANYL ISOCYANATE, with the molecular formula C10H7NO and a molecular weight of 157.17 g/mol, is an isocyanate derivative featuring a chiral center. This characteristic leads to the existence of two stereoisomers. It is a highly reactive chemical compound, which necessitates careful handling and precautions during its use.
Uses
Used in Organic Synthesis:
(R)-(-)-1-INDANYL ISOCYANATE is used as a reagent in the organic synthesis industry for the formation of isocyanate-containing compounds. Its application is crucial in creating materials such as polyurethanes, which are versatile polymers with a wide range of applications, including foams, elastomers, and coatings.
Used in Pharmaceutical Production:
In the pharmaceutical industry, (R)-(-)-1-INDANYL ISOCYANATE is utilized as a key compound in the development and production of various medications. Its reactivity and structural properties make it a valuable component in the synthesis of biologically active compounds, contributing to the creation of new and improved drugs.
Used in Agrochemical Production:
(R)-(-)-1-INDANYL ISOCYANATE also finds application in the agrochemical sector, where it is employed in the synthesis of chemicals used in agriculture. These can include pesticides, herbicides, and other compounds that help protect crops and enhance agricultural productivity. Its role in this industry is significant, as it contributes to the development of effective and targeted agrochemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 745783-80-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,4,5,7,8 and 3 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 745783-80:
(8*7)+(7*4)+(6*5)+(5*7)+(4*8)+(3*3)+(2*8)+(1*0)=206
206 % 10 = 6
So 745783-80-6 is a valid CAS Registry Number.
745783-80-6Relevant articles and documents
Enantioselective Aza-Henry reaction with an N-sulfinyl urea organocatalyst
Robak, Maryann T.,Trincado, Monica,Ellman, Jonathan A.
, p. 15110 - 15111 (2008/09/18)
A new class of organocatalyst has been developed that incorporates a sulfinyl group as a urea or thiourea substituent. The sulfinyl group serves to simultaneously acidify the urea and provide asymmetric induction in hydrogen-bond-catalyzed reactions. The utility of this new catalyst structure is demonstrated by the high selectivity provided in the aza-Henry reaction not only for aromatic N-Boc imine substrates but also for aliphatic imines for which enantioselective H-bonding catalysis has not previously been demonstrated. Copyright
