6021-32-5 Usage
Uses
Used in Pharmaceutical Industry:
Methyl 4-bromo-2,3-dimethylbenzoate is used as a synthetic intermediate for the production of pharmaceuticals. Its unique structure allows it to be a key component in the creation of various medicinal compounds, contributing to the development of new drugs and therapies.
Used in Agrochemical Industry:
In the agrochemical sector, Methyl 4-bromo-2,3-dimethylbenzoate serves as an intermediate in the synthesis of agrochemicals. Its role in this industry is crucial for the development of pesticides and other agricultural chemicals that protect crops and enhance agricultural productivity.
Used in Perfumery:
Methyl 4-bromo-2,3-dimethylbenzoate is used as a component in the production of perfumes due to its strong and distinctive odor. Its aromatic properties make it a valuable addition to the fragrance industry, where it contributes to the creation of various scent profiles.
Used in Flavoring Agents:
Methyl 4-bromo-2,3-dimethylbenzoate is also utilized in the flavor industry, where it is employed to enhance or create specific taste profiles in food products. Its unique flavor characteristics make it a useful tool for flavor chemists in developing new and innovative flavor combinations.
Check Digit Verification of cas no
The CAS Registry Mumber 6021-32-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,2 and 1 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6021-32:
(6*6)+(5*0)+(4*2)+(3*1)+(2*3)+(1*2)=55
55 % 10 = 5
So 6021-32-5 is a valid CAS Registry Number.
InChI:InChI=1/C23H17N3O4/c1-15-9-11-17(23-25-19-7-2-3-8-21(19)30-23)14-20(15)24-22(27)12-10-16-5-4-6-18(13-16)26(28)29/h2-14H,1H3,(H,24,27)/b12-10+
6021-32-5Relevant academic research and scientific papers
A conjunctive diiodoheptaene for the synthesis of C2-symmetric carotenoids
Fontán, Noelia,Vaz, Belén,álvarez, Rosana,De Lera, ángel R.
supporting information, p. 2694 - 2696 (2013/04/10)
(2E,4E,6E,8E,10E,12E,14E)-2,15-Diiodo-6,11-dimethylhexadeca-2,4,6,8,10,12, 14-heptaene, prepared by homometathesis, has been used in palladium-catalyzed Suzuki and Stille cross-coupling reactions with the appropriate partners to construct the C2-symmetric carotenoids β,β-carotene, lycopene, synechoxanthin and 4,4′-diapo-ψ,ψ-carotene-4,4′- dial. The Royal Society of Chemistry 2013.
