6291-15-2 Usage
Uses
Used in Food Industry:
3-tert-butyl-2-hydroxy-5-methoxybenzoic acid is used as a food preservative for its ability to prevent oxidation and rancidity in food products, which helps to extend their shelf life.
Used in Cosmetics and Pharmaceuticals:
3-tert-butyl-2-hydroxy-5-methoxybenzoic acid is used as an antioxidant in cosmetics and pharmaceuticals due to its ability to prevent oxidation and protect against free radicals.
However, it is important to note that there is some controversy surrounding the safety of BHA, with concerns about its potential carcinogenicity and potential adverse effects on human health. Further research and evaluation are needed to fully understand the risks and benefits of using BHA in various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 6291-15-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,9 and 1 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6291-15:
(6*6)+(5*2)+(4*9)+(3*1)+(2*1)+(1*5)=92
92 % 10 = 2
So 6291-15-2 is a valid CAS Registry Number.
InChI:InChI=1/C12H16O4/c1-12(2,3)9-6-7(16-4)5-8(10(9)13)11(14)15/h5-6,13H,1-4H3,(H,14,15)
6291-15-2Relevant academic research and scientific papers
Yang, Jenny Y.,Nocera, Daniel G.
, p. 4796 - 4798 (2008)
A modular ligand macrocycle is composed from two phenolic groups linked to a cyclohexane bridge through an amide bond and an imine bond. The stability of the asymmetric linkers to metathesis permits a macrocyclic platform to be assembled from the condensation of two different phenolic groups in a single-step, high yield, reaction. The primary coordination sphere may be tuned with functional groups on one phenolic group. The other phenolic group may be modified with a scaffold possessing a proton transfer group. In this way, control over the secondary coordination sphere of the macrocycle is achieved. Manganese complexes of the amido-imine linked macrocycle catalytically epoxidizes 1,2-dihydronapthalene using sodium hypochlorite as the oxidant. The amido-imine macrocycles represent a new metal active site capable of supporting high oxidation states and attendant atom transfer chemistry while at the same time permitting control over the primary and secondary sphere of the metal center.
