78843-64-8 Usage
Description
(R)-(+)-1,2-HEPTANEDIOL is a chiral compound that consists of a heptane backbone with two hydroxyl groups attached at the 1 and 2 positions. It is known for its ability to influence the enantioselectivity of reactions, making it a valuable tool in the production of optically pure compounds. Additionally, it has been studied for its antimicrobial and antifungal properties, making it a versatile and important chemical in various industries.
Uses
Used in Pharmaceutical Industry:
(R)-(+)-1,2-HEPTANEDIOL is used as a chiral building block for the synthesis of various pharmaceuticals. Its ability to influence the enantioselectivity of reactions is crucial in producing optically pure compounds, which are essential for the development of effective and safe medications.
Used in Agrochemical Industry:
(R)-(+)-1,2-HEPTANEDIOL is used as a chiral building block in the production of agrochemicals. Its enantioselective properties are valuable in creating optically pure compounds that can be more effective and selective in their action, reducing potential environmental impact.
Used in Fragrance Industry:
(R)-(+)-1,2-HEPTANEDIOL is used as a chiral building block in the synthesis of fragrances. The enantioselective nature of the compound allows for the creation of specific scents that can be more appealing and have a greater impact on the desired olfactory experience.
Used in Antimicrobial Applications:
(R)-(+)-1,2-HEPTANEDIOL is used as an antimicrobial agent due to its studied properties against certain microorganisms. This application can be found in various industries, such as healthcare and food preservation, where controlling the growth of harmful microorganisms is essential.
Used in Antifungal Applications:
(R)-(+)-1,2-HEPTANEDIOL is used as an antifungal agent, making it a valuable component in products that aim to prevent or treat fungal infections. This application can be found in the medical, agricultural, and personal care industries, where controlling fungal growth is important for health and safety.
Check Digit Verification of cas no
The CAS Registry Mumber 78843-64-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,8,4 and 3 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 78843-64:
(7*7)+(6*8)+(5*8)+(4*4)+(3*3)+(2*6)+(1*4)=178
178 % 10 = 8
So 78843-64-8 is a valid CAS Registry Number.
78843-64-8Relevant articles and documents
An enantioselective approach to 2-alkyl substituted tetrahydroquinolines: Total synthesis of (+)-angustureine
Garg, Yuvraj,Gahalawat, Suraksha,Pandey, Satyendra Kumar
, p. 38846 - 38850 (2015/05/20)
A simple and highly efficient synthetic approach to enantiopure 2-alkyl substituted tetrahydroquinoline 1 skeleton from aldehydes as starting materials and its application to the total synthesis of (+)-angustureine 2 is described. Key transformations incl
Synthesis of substituted α,β-unsaturated δ-lactones from vinyl tellurides
Oliveira, Juliana M.,R. Freitas, Juliano C.,Comasseto, Jo?o Valdir,Menezes, Paulo Henrique
experimental part, p. 3003 - 3009 (2011/04/27)
A new approach for the synthesis of α,β-unsaturated δ-lactones, a unit present in many natural products with interesting biological activities is described. The approach was based on the use of a vinyl telluride, and it is complementary to the methods usi
A route to 1,2-diols by enantioselective organocatalytic α-oxidation with molecular oxygen
Ibrahem, Ismail,Zhao, Gui-Ling,Sundén, Henrik,Córdova, Armando
, p. 4659 - 4663 (2007/10/03)
A route to 1,2-diols by the direct organocatalytic enantioselective α-oxidation of aldehydes using molecular oxygen is presented. Protected commercially available chiral pyrrolidines catalyze the asymmetric α-oxidation of aldehydes with singlet molecular oxygen with high enantioselectivity to furnish the corresponding diols after in situ reduction in high yield with up to 98% ee. Electrophilic singlet molecular oxygen was photo or chemically generated ('dark' 1O2).