2-Methyl-2-oxazoline

2-Methyl-4,5-dihydrooxazole

What is 2-Methyl-2-oxazoline, cas no. 1120-64-5,a producer telling you the result.

                                                                CAS NO. 1120-64-5

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To begin with, let us tell you what is the basic information of 2-Methyl-2-oxazoline CAS NO. 1120-64-5 ?

Molecular Formula

C4H7NO

Molecular Weight

85.104

Density

1.1±0.1 g/cm3

Boiling Point

110.0±0.0 °C at 760 mmHg

Flash Point

20.0±0.0 °C

Exact Mass

85.052765

EINECS

214-316-3

MD NO.

MFCD00005298

 

Like many stuff, it has many synonyms as follows

Oxazole, 4,5-dihydro-2-methyl-

2-Methyloxazoline

2-Methyl-4,5-dihydro-1,3-oxazole

2-Methyl-4,5-dihydrooxazole

2-Methyl-2-oxazoline

First, the chemical is very special, some technical indexes as below

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Physical property data

1. Appearance: Liquid.

2. Density (g/mL, 25 ): 1.005

3. Relative vapor density (g/mL, air=1): not determined

4. Melting point (º C): undetermined

5. Boiling point (º C, atmospheric pressure): 109.5-110.5

6. Boiling point (º C, 749mmHg): undetermined

7. Refractive index (n20/D): 1.434

8. Flash point (º C): 20

9. Specific rotation (º): not determined

10. Spontaneous combustion point or ignition temperature (º C): not determined

11. Vapor pressure (psi, 20 º C): not determined

12. Saturated vapor pressure (kPa, 60 º C): not determined

13. Combustion heat (KJ/mol): undetermined

14. Critical temperature (º C): not determined

15. Critical pressure (KPa): undetermined

16. Logarithmic value of oil-water (octanol/water) partition coefficient: undetermined

17. Explosion upper limit (%, V/V): undetermined

18. Lower explosive limit (%, V/V): not determined

19. Solubility: undetermined

toxicology data

Skin and mucous membranes have irritant effects

Ecological data

Slightly harmful to water, do not allow undiluted or large amounts of products to come into contact with groundwater, waterways, or sewage systems. Do not discharge materials into the surrounding environment without government permission

Molecular structure data

1. Molar refractive index: 22.68

2. Molar volume (m3/mol): 78.0

3. Waiting for Zhang Biarong (90.2K): 185.3

4. Surface tension (dyne/cm): 31.7

5. Dielectric constant: not available

6. Bipolar distance (10-24cm3): not available

7. Polarization rate: 8.99

Calculate chemical data

1. Reference value for hydrophobic parameter calculation (XlogP): -0.2

2. Number of hydrogen bond donors: 0

3. Number of hydrogen bond acceptors: 2

4. Number of rotatable chemical bonds: 0

5. Number of tautomers: None

6. Topological molecular polarity surface area 21.6

7. Number of heavy atoms: 6

8. Surface charge: 0

9. Complexity: 77.6

10. Number of isotopic atoms: 0

11. Determine the number of atomic stereocenters: 0

12. Uncertain number of atomic stereocenters: 0

13. Determine the number of chemical bond stereocenters: 0

14. Number of uncertain chemical bond stereocenters: 0

15. Number of covalent bond units: 1

Nature and stability

Stable at room temperature and pressure, avoiding contact with oxides

Storage method

Keep the container sealed and store in a cool, dry place

 

Second, the Synthetic Route we will recommend is the most important for your reference?

First, synthesis line of 2-Methyl-2-oxazoline CAS NO. 1120-64-5  as follows

The compound with CAS number 1120-64-5 is 2-methyl-2-oxazoline (also known as 2-methyl-2-oxazoline), which has multiple synthetic routes. Here are some known synthetic routes:

1. Synthesis route reported in literature:

According to the search results, there are at least 11 different synthetic routes, which are detailed in academic journals such as Journal of the American Chemical Society, Journal of Organic Chemistry, and Synthesis. ‌

The specific synthesis efficiency can reach about 75%. ‌

2. Common synthesis methods:

The usual synthesis method is to obtain 2 through the oxidation reaction of 2-amino-2-methyl-1-propene. ‌

3. Other possible synthetic pathways:

Due to the diversity and complexity of synthetic routes, there may be other synthesis methods that have not been detailed. These methods may involve different starting materials, catalysts, and reaction conditions. ‌

 

Third, what is the usage of  2-Methyl-2-oxazoline  CAS NO. 1120-64-5  pleas see below

 

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2-methyl-2-azoline has a wide range of applications in many fields. It is often used as a catalyst, organic solvent, and inhibitor. In terms of organic solvents, it can be used to dissolve many organic compounds. In addition, 2-methyl-2-azoline is widely used in industrial processes such as coatings, rubber processing, synthetic fibers, and metal cleaning.

 

Other usages as below

 

Used for the synthesis of  2-(2,5-dioxopyrrolidin-1-yl)ethyl acetate

 

Cas no. 28833-81-0

 

Used for the synthesis of  
7a-methyl-6-(phenoxymethyl)-2,3,5,6-tetrahydro-[1,3]oxazolo[2,3-b][1,3]oxazole

 

Cas no. 13488-71-6

 

Used for the synthesis of N-(2-Chloroethyl)acetamide
 

,Cas no. 7355-58-0

 

Besides Safety Information of 2-Methyl-2-oxazoline  CAS NO.1120-64-5  is also important when handling it

 

Hazard Codes 

Xi

WGK Germany 

3

HSCode

2934999090

TSCA 

Yes

HazardClass 

IRRITANT

 

 

What is the appearance of 2-Methyl-2-oxazoline  CAS NO.1120-64-5?   Please see the picture of 2-Methyl-2-oxazoline  CAS NO.1120-64-5, below

 

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Specification of 2-Methyl-2-oxazoline  CAS NO.1120-64-5, is below

Apperance: Clear colorless to very faint yellow liquid

Assay: 99 min  by GC

IR identity: conform

Water:0.5% max by K.F.

HNMR  picture of  2-Methyl-2-oxazoline  CAS NO.1120-64-5   is as follows,

IR  picture of  2-Methyl-2-oxazoline  CAS NO.1120-64-5   is as follows,

Reference of  Article cited for your reference below,

(1)

Unnatural biopolymers of saccharides and proteins conjugated with poly(2-oxazoline) and methacrylate-based polymers: from polymer design to bioapplication

Publication Date: 2022

Publication Name: Polymer Journal

(2)

Cationic Graft Polymerization onto Silica Nanoparticle Surface in a Solvent-Free Dry-System

Publication Date: 2008

Publication Name: Polymer Bulletin

(3)

Copolymerization via zwitterion

Publication Date: 1984

Publication Name: Polymer Bulletin