5309-42-2 Usage
General Description
(-)-D-Glycerol 1-butyrate, also known as (-)-DGHB, is a chemical compound that belongs to the class of organic compounds known as monosaccharides. It is a derivative of glycerol and is commonly used as a food additive and flavoring agent, as well as in pharmaceutical and cosmetic products. (-)-DGHB is used as a stabilizer, thickener, and emulsifier in food and beverage products, and has potential therapeutic applications in the treatment of inflammatory diseases and metabolic disorders. It is also used as a precursor in the synthesis of various pharmaceutical drugs and has shown promising results in clinical research as a potential anti-inflammatory and anti-cancer agent. Overall, (-)-D-Glycerol 1-butyrate is a versatile and important chemical compound with a wide range of industrial and medical applications.
Check Digit Verification of cas no
The CAS Registry Mumber 5309-42-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,0 and 9 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5309-42:
(6*5)+(5*3)+(4*0)+(3*9)+(2*4)+(1*2)=82
82 % 10 = 2
So 5309-42-2 is a valid CAS Registry Number.
5309-42-2Relevant articles and documents
Dinuclear salen cobalt complex incorporating Y(OTf)3: enhanced enantioselectivity in the hydrolytic kinetic resolution of epoxides
Patel, Deepak,Kurrey, Ganesh Ram,Shinde, Sandip S.,Kumar, Pradeep,Kim, Geon-Joong,Thakur, Santosh Singh
, p. 82699 - 82703 (2015/10/19)
The activation of inactive Jacobsen's chiral salen Co(ii) (salen = N,N′-bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexanediamine) compound is attained by dinuclear chiral salen Co(iii)-OTf complex formation with yttrium triflate. The yttrium metal not only displays a promoting effect on electron transfer, but also assists in forming two stereocentres of a Lewis acid complex with Co(iii)-OTf. We found that the binuclear Co-complex significantly enhanced reactivity and enantioselectivity in the hydrolytic kinetic resolution of terminal epoxides compared to its analogous monomer and kinetic data are also consistent with these results.
