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Key Documents

419885

Sigma-Aldrich

tert-Butyl propiolate

98%

Synonym(s):

tert-Butyl acetylenecarboxylate

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About This Item

Linear Formula:
HC≡CCOOC(CH3)3
CAS Number:
Molecular Weight:
126.15
Beilstein:
1747175
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

98%

form

liquid

refractive index

n20/D 1.418 (lit.)

bp

52-53 °C/27 mmHg (lit.)

mp

18-20 °C (lit.)

density

0.919 g/mL at 25 °C (lit.)

SMILES string

CC(C)(C)OC(=O)C#C

InChI

1S/C7H10O2/c1-5-6(8)9-7(2,3)4/h1H,2-4H3

InChI key

XGTPDIIFEPTULX-UHFFFAOYSA-N

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General description

tert-Butyl propiolate is an ester. It reacts with methimazole to afford tert-butyl (E)-3-(1-methyl-1H-imidazol-2-ylthio) acrylate. Crystallographic data for the lithium enolate of tert-butyl propiolate has been described..

Application

tert-Butyl propiolate may be used in the preparation of heterocycles, alkaloids, and unsaturated amino acids.

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

Pictograms

FlameExclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

82.4 °F - closed cup

Flash Point(C)

28 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Tetrahedron, 48, 669-669 (1992)
Structures of three lithium ester enolates by X-ray diffraction: derivation of reaction path for cleavage into ketene and alcoholate.
Seebach D, et al.
Journal of the American Chemical Society, 170(19), 5403-5409 (1985)
Tetrahedron Letters, 30, 3625-3625 (1989)
Christopher M Hattan et al.
Synthetic communications, 43(1), 1-8 (2013-01-01)
The syntheses of 3-(1-methyl-1
Journal of the American Chemical Society, 112, 7682-7682 (1990)

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