Cyclohexylboronic acid pinacol ester

• CAS: 87100-15-0
• Catalog Number: ACM87100150
• Category: Boronic Esters
• Molecular Weight: 210.12
• Molecular Formula: C₁₂H₂₃BO₂

Custom Q&A

What is the molecular formula of Cyclohexylboronic acid pinacol ester?

The molecular formula of Cyclohexylboronic acid pinacol ester is C12H23BO2.

What is the molecular weight of Cyclohexylboronic acid pinacol ester?

The molecular weight of Cyclohexylboronic acid pinacol ester is 210.12 g/mol.

What is the IUPAC name of Cyclohexylboronic acid pinacol ester?

The IUPAC name of Cyclohexylboronic acid pinacol ester is 2-cyclohexyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane.

What is the InChI of Cyclohexylboronic acid pinacol ester?

The InChI of Cyclohexylboronic acid pinacol ester is InChI=1S/C12H23BO2/c1-11(2)12(3,4)15-13(14-11)10-8-6-5-7-9-10/h10H,5-9H2,1-4H3.

What is the InChIKey of Cyclohexylboronic acid pinacol ester?

The InChIKey of Cyclohexylboronic acid pinacol ester is OUEVCDGYTKLNMJ-UHFFFAOYSA-N.

What is the canonical SMILES representation of Cyclohexylboronic acid pinacol ester?

The canonical SMILES representation of Cyclohexylboronic acid pinacol ester is B1(OC(C(O1)(C)C)(C)C)C2CCCCC2.

What is the CAS number of Cyclohexylboronic acid pinacol ester?

The CAS number of Cyclohexylboronic acid pinacol ester is 87100-15-0.

What is the EC number of Cyclohexylboronic acid pinacol ester?

The EC number of Cyclohexylboronic acid pinacol ester is 814-148-6.

What is the hydrogen bond donor count of Cyclohexylboronic acid pinacol ester?

The hydrogen bond donor count of Cyclohexylboronic acid pinacol ester is 0.

What is the hydrogen bond acceptor count of Cyclohexylboronic acid pinacol ester?

The hydrogen bond acceptor count of Cyclohexylboronic acid pinacol ester is 2.

Synthetic Use

Upstream Synthesis Route 1

• 76-09-5
• 4441-56-9

• 87100-15-0

Reference: [1] Journal of the American Chemical Society, 2012, vol. 134, # 27, p. 11298 - 11298

Upstream Synthesis Route 2

• 24388-23-6

• 87100-15-0

Reference: [1] Patent: US2018/51042, 2018, A1, . Location in patent: Paragraph 0065

Upstream Synthesis Route 3

• 108-85-0
• 73183-34-3

• 87100-15-0

Reference: [1] Organic Letters, 2012, vol. 14, # 3, p. 890 - 893

Upstream Synthesis Route 4

• 76-09-5
• 32999-09-0

• 87100-15-0

Reference: [1]Journal of the American Chemical Society,2007,vol. 129,p. 3068 - 3069

Downstream Synthesis Route 1

• 1088-01-3
• 67-63-0

• 87100-15-0

Reference: [1]Journal of the Chemical Society. Chemical communications,1977,p. 690 - 691

* For details of the synthesis route, please refer to the original source to ensure accuracy.