4433-63-0 Usage
Description
Ethylboronic acid, also known as boronic acid, is an organic compound with the chemical formula C2H5B(OH)2. It is a colorless liquid that is soluble in water and has a mild, acidic taste. Ethylboronic acid is known for its ability to form stable complexes with various organic compounds, making it a versatile chemical intermediate in the synthesis of various organic and inorganic compounds.
Uses
Used in Chemical Synthesis:
Ethylboronic acid is used as a chemical intermediate for the synthesis of various organic and inorganic compounds. Its ability to form stable complexes with organic compounds makes it a valuable reagent in the preparation of a wide range of chemical products.
Used in Material Science:
Ethylboronic acid is used as the sole precursor in the successful preparation of boron-doped graphene (B-doped graphene) films with large areas. B-doped graphene is a promising material with enhanced electrical and mechanical properties, making it suitable for various applications in the electronics and energy storage industries.
Check Digit Verification of cas no
The CAS Registry Mumber 4433-63-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,3 and 3 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4433-63:
(6*4)+(5*4)+(4*3)+(3*3)+(2*6)+(1*3)=80
80 % 10 = 0
So 4433-63-0 is a valid CAS Registry Number.
InChI:InChI=1/C2H7BO2/c1-2-3(4)5/h4-5H,2H2,1H3
4433-63-0Relevant articles and documents
The preparation of pentafluorophenyldihaloboranes from pentafluorophenylmercurials C6F5HgR and BX3: the dramatic dependence of the reaction direction on the ligand R
Bardin, Vadim V.,Adonin, Nicolay Yu.
, p. 1523 - 1531 (2019/07/22)
Abstract: In search of convenient preparations of C6F5BX2 (X = Cl, Br), reactions of C6F5HgR (R = C6F5, C6H5, C2H5, Br and Cl) with BX3 were studied. Under the action of BCl3 the order of the C–Hg bond cleavage is C6F5Hg–C6H5 > C6F5–HgC2H5 > C6F5–HgC6F5 >> C6F5–HgCl. With more reactive BBr3 the sequence is C6F5Hg–C6H5 > C6F5–HgC2H5 ~ C6F5Hg–C2H5 > C6F5–HgC6F5 ≥ C6F5–HgBr. During the study we found the simple way to alkyldibromoboranes which is presented by the preparation of C2H5BBr2 from C2H5HgBr and BBr3. It is the second example of synthesis of alkylmercury derivative in an addition to the earlier reported formation of cyclopropylmercurials from di(cyclopropyl)mercury and BX3. Graphic abstract: [Figure not available: see fulltext.].
