Structure

3-Bromomethyl-3-methyloxetane

CAS
78385-26-9
Catalog Number
ACM78385269
Category
Other Products
Molecular Weight
165.03
Molecular Formula
C5H9BrO

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Specification

Synonyms
BUTTPARK 89\10-22;3-BROMOMETHYL-3-METHYLOXETANE;Oxetane, 3-(bromomethyl)-3-methyl- (9CI);3-methyl-3-bromomethyloxetane;3-Bromomethyl-3-methyloxe...;3-BroMoMethyl-3-Methyloxetane Oxetane, 3-(broMoMethyl)-3-Methyl-;Oxetane, 3-(broMoMethyl)-3-Methyl-
Boiling Point
162°C
Flash Point
62°C
Density
1.438
Hazard Statements
Xn
What is the molecular formula of 3-Bromomethyl-3-methyloxetane?

The molecular formula of 3-Bromomethyl-3-methyloxetane is C5H9BrO.

When was 3-Bromomethyl-3-methyloxetane first created?

3-Bromomethyl-3-methyloxetane was first created on August 8, 2005.

What is the molecular weight of 3-Bromomethyl-3-methyloxetane?

The molecular weight of 3-Bromomethyl-3-methyloxetane is 165.03 g/mol.

What is the IUPAC name of 3-Bromomethyl-3-methyloxetane?

The IUPAC name of 3-Bromomethyl-3-methyloxetane is 3-(bromomethyl)-3-methyloxetane.

How many Hydrogen Bond Acceptor Counts does 3-Bromomethyl-3-methyloxetane have?

3-Bromomethyl-3-methyloxetane has 1 Hydrogen Bond Acceptor Count.

What is the XLogP3-AA value of 3-Bromomethyl-3-methyloxetane?

The XLogP3-AA value of 3-Bromomethyl-3-methyloxetane is 1.3.

What is the exact mass of 3-Bromomethyl-3-methyloxetane?

The exact mass of 3-Bromomethyl-3-methyloxetane is 163.98368 g/mol.

How many Covalently-Bonded Unit Counts does 3-Bromomethyl-3-methyloxetane have?

3-Bromomethyl-3-methyloxetane has 1 Covalently-Bonded Unit Count.

Is 3-Bromomethyl-3-methyloxetane the canonicalized compound?

Yes, 3-Bromomethyl-3-methyloxetane is the canonicalized compound.

What is the InChIKey of 3-Bromomethyl-3-methyloxetane?

The InChIKey of 3-Bromomethyl-3-methyloxetane is MGBZKWOJRYGRTO-UHFFFAOYSA-N.

Upstream Synthesis Route 1

  • 3143-02-0
  • 78385-26-9

Reference: [1] Journal of Organic Chemistry, 1998, vol. 63, # 11, p. 3631 - 3646

Upstream Synthesis Route 2

  • 77-85-0
  • 78385-26-9

Reference: [1] Acta Chemica Scandinavica, 1991, vol. 45, # 1, p. 82 - 91
[2] Journal of Fluorine Chemistry, 2016, vol. 190, p. 75 - 80
[3] Chemistry of Heterocyclic Compounds, 2017, vol. 53, # 6-7, p. 811 - 821[4] Khim. Geterotsikl. Soedin., 2017, vol. 53, # 6-7, p. 811 - 821,11

Upstream Synthesis Route 3

  • 99314-44-0
  • 78385-26-9

Reference: [1] Journal of Organic Chemistry, 1998, vol. 63, # 11, p. 3631 - 3646
[2] Patent: EP1927592, 2008, A1, . Location in patent: Page/Page column 11
[3] Bulletin of the Chemical Society of Japan, 2011, vol. 84, # 1, p. 26 - 39
[4] Tetrahedron, 2002, vol. 58, # 35, p. 7049 - 7064
[5] Patent: WO2018/75698, 2018, A1, . Location in patent: Paragraph 00272

Upstream Synthesis Route 4

  • 3143-02-0
  • 78385-26-9

Reference: [1]Journal of Organic Chemistry,1998,vol. 63,p. 3631 - 3646

Downstream Synthesis Route 1

  • 78385-26-9
  • 112-35-6
  • 697799-20-5

Reference: [1]Tetrahedron,1993,vol. 49,p. 5869 - 5872

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

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