79762-78-0 Usage
Description
ALPHA-BROMO-TERT-BUTYL ACRYLATE, 95% is a colorless liquid chemical compound with a distinct acrid odor, known for its high flammability and ability to polymerize at elevated temperatures. It serves as a crucial building block in the manufacturing of polymers and other industrial products, playing a significant role in the development of various advanced materials.
Uses
Used in Polymer Manufacturing Industry:
ALPHA-BROMO-TERT-BUTYL ACRYLATE, 95% is used as a monomer for the synthesis of polymers due to its ability to polymerize at elevated temperatures. This property allows it to contribute to the creation of a wide range of polymers with diverse applications in various industries.
Used in Advanced Material Production:
ALPHA-BROMO-TERT-BUTYL ACRYLATE, 95% is used as a building block for the development of advanced materials. Its reactivity and polymerization capabilities make it a valuable component in the production of materials with specific properties required for high-performance applications.
Used in Industrial Product Formulation:
ALPHA-BROMO-TERT-BUTYL ACRYLATE, 95% is used as a key ingredient in the formulation of various industrial products. Its unique chemical properties enable it to enhance the performance and characteristics of these products, making them suitable for specialized applications.
It is important to handle ALPHA-BROMO-TERT-BUTYL ACRYLATE, 95% with caution due to its hazardous nature if not managed properly. Proper safety measures should be taken during its use to ensure the safety of individuals and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 79762-78-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,7,6 and 2 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 79762-78:
(7*7)+(6*9)+(5*7)+(4*6)+(3*2)+(2*7)+(1*8)=190
190 % 10 = 0
So 79762-78-0 is a valid CAS Registry Number.
InChI:InChI=1/C7H11BrO2/c1-5(8)6(9)10-7(2,3)4/h1H2,2-4H3
79762-78-0Relevant articles and documents
How Reaction Conditions May Influence the Regioselectivity in the Synthesis of 2,3-Dihydro-1,4-benzoxathiine Derivatives
Casiraghi, Andrea,Valoti, Ermanno,Suigo, Lorenzo,Artasensi, Angelica,Sorvillo, Erica,Straniero, Valentina
, p. 13217 - 13227 (2018/10/24)
The exploration of different reaction conditions aiming to obtain both 2,3-dihydro-1,4-benzoxathiine-2-yl derivatives and 2,3-dihydro-1,4-benzoxathiine-3-yl ones is reported. The treatment of 1,2-mercaptophenol with an organic base and a specific 2-bromo acrylate results in a solvent- and substrate-dependent exclusive solvation of O- and S-anions, thus managing the regioselectivity.
Mechanism-based inactivation of coenzyme B12-dependent 2-methyleneglutarate mutase by (Z)-glutaconate and buta-1,3-diene-2,3- dicarboxylate
Buckel, Wolfgang,Pierik, Antonio J.,Plett, Sandra,Alhapel, Ashraf,Suarez, Diana,Tu, Shang-Min,Golding, Bernard T.
, p. 3622 - 3626 (2007/10/03)
In the presence of holo 2-methyleneglutarate mutase, buta-1,3-diene-2,3- dicarboxylate and (Z)-glutaconate [(Z)-pent-2-ene-1,5-dicarboxylate], but not (E)-glutaconate, each induced homolysis of the Co-C bond of coenzyme B 12 to afford cob(II)alamin and the 5′-deoxyadenosyl radical. The latter probably added to the double bond in (Z)-glutaconate and one of the double bonds in buta-1,3-diene-2,3-dicarboxylate to afford a corresponding "radical adduct". The formation of new radicals and cob(II)alamin was diagnosed by UV/Visible and EPR spectroscopy. (Z)-Glutaconate rapidly inactivated the mutase with formation of aquocobalamin, which was possibly derived by electron transfer from cob(II)alamin to the radical adduct. In contrast, buta-1,3-diene-2,3-dicarboxylate was a much slower inactivator. In this case, the spectroscopic data revealed a relatively stable complex of the radical adduct with cob(II)alamin in the active site of the enzyme. Wiley-VCH Verlag GmbH & Co. KGaA, 2006.
