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Merck
모든 사진(1)

문서

09954

Sigma-Aldrich

Propargyl p-toluenesulfonate

≥97.0% (GC)

동의어(들):

Propargyl tosylate

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About This Item

실험식(Hill 표기법):
C10H10O3S
CAS Number:
Molecular Weight:
210.25
Beilstein:
1912957
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22

분석

≥97.0% (GC)

refractive index

n20/D 1.530

density

1.215 g/mL at 20 °C (lit.)

저장 온도

2-8°C

SMILES string

Cc1ccc(cc1)S(=O)(=O)OCC#C

InChI

1S/C10H10O3S/c1-3-8-13-14(11,12)10-6-4-9(2)5-7-10/h1,4-7H,8H2,2H3

InChI key

LMBVCSFXFFROTA-UHFFFAOYSA-N

애플리케이션

Propargyl p-toluenesulfonate can be used as an initiator in the synthesis of linear and cyclic poly(2-isopropyl-2-oxazoline)s by cationic ring-opening polymerization of 2-isopropyl-2-oxazoline.
It can also be used as a reagent to synthesize:
  • 2-hydroxy-4-pentynoic acid by an alkylation reaction with diethyl 2-acetamidomalonate followed by subsequent hydrolysis, decarboxylation, diazotization, and hydroxylation reactions.
  • Furan derivatives by Pd-catalyzed reaction with acylchromates.

픽토그램

Exclamation mark

신호어

Warning

유해 및 위험 성명서

Hazard Classifications

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

표적 기관

Respiratory system

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point (°F)

212.0 °F - closed cup

Flash Point (°C)

100 °C - closed cup

개인 보호 장비

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


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Linear and cyclic poly (2-isopropyl-2-oxazoline) s for fine control of thermoresponsiveness
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Preparation of furans by palladium-catalyzed reaction of acylchromates and propargylic tosylates
Nakamura M, et al.
Heterocycles, 59(1), 333-345 (2003)
An economical and safe procedure to synthesize 2-hydroxy-4-pentynoic acid: A precursor towards `clickable?biodegradable polylactide
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