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178748

Sigma-Aldrich

2,4,4-Trimethyl-2-oxazoline

98%

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Empirical Formula (Hill Notation):
C6H11NO
CAS Number:
Molecular Weight:
113.16
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.22

assay

98%

form

liquid

refractive index

n20/D 1.4213 (lit.)

bp

112-113 °C (lit.)

density

0.887 g/mL at 25 °C (lit.)

SMILES string

CC1=NC(C)(C)CO1

InChI

1S/C6H11NO/c1-5-7-6(2,3)4-8-5/h4H2,1-3H3

InChI key

HZRZMHNRCSIQFT-UHFFFAOYSA-N

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This Item
405973219185137448
vibrant-m

178748

2,4,4-Trimethyl-2-oxazoline

vibrant-m

219185

2,4,5-Trimethylthiazole

vibrant-m

137448

2-Methyl-2-oxazoline

refractive index

n20/D 1.4213 (lit.)

refractive index

-

refractive index

n20/D 1.509 (lit.)

refractive index

n20/D 1.434 (lit.)

bp

112-113 °C (lit.)

bp

-

bp

166-167 °C/717 mmHg (lit.)

bp

109.5-110.5 °C (lit.)

density

0.887 g/mL at 25 °C (lit.)

density

-

density

1.013 g/mL at 25 °C (lit.)

density

1.005 g/mL at 25 °C (lit.)

form

liquid

form

solid

form

liquid

form

liquid

Application

2,4,4-Trimethyl-2-oxazoline was used in the synthesis of 2,2-dimethyloxazolines of C2-elongated fatty acids.

pictograms

Flame

signalword

Danger

hcodes

pcodes

Hazard Classifications

Flam. Liq. 2

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

55.4 °F - closed cup

flash_point_c

13 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


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Dmitry V Kuklev et al.
Chemistry and physics of lipids, 144(2), 172-177 (2006-10-20)
Three fatty acids were synthesized from commercially available alpha-linolenic, stearidonic and eicosapentaenoic acids by C2-elongation using a four step preparative technique. The parent fatty acid methyl esters were reduced to alcohols with LiAlH(4), converted to bromides by treatment with triphenylphosphine
Po-Jung Tsai et al.
Inflammation, 41(4), 1200-1214 (2018-03-29)
Juniperonic acid (JPA; Δ5,11,14,17-20:4), originally identified in certain gymnosperm seeds, is a rare n-3 polyunsaturated fatty acid (PUFA) with lipid-modulating effects on rats and anti-proliferative effects on fibroblast cell proliferation. However, little is known how JPA exerted its immunosuppressive effect.

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