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Merck
모든 사진(2)

주요 문서

791571

Sigma-Aldrich

Isopropyl p-toluenesulfonate

97%

동의어(들):

Isopropyl p-tosylate

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모든 사진(2)

About This Item

실험식(Hill 표기법):
C10H14O3S
CAS Number:
2307-69-9
Molecular Weight:
214.28
EC Number:
218-989-4
MDL number:
MFCD00968877
UNSPSC 코드:
12352100
NACRES:
NA.22

Quality Level

100

분석

97%

양식

liquid

refractive index

n20/D 1.503

density

1.142 g/mL at 25 °C

저장 온도

2-8°C

SMILES string

[S](=O)(=O)(Oc1ccc(cc1)C)C(C)C

InChI

1S/C10H14O3S/c1-8(2)14(11,12)13-10-6-4-9(3)5-7-10/h4-8H,1-3H3

InChI key

MUTOLSSCMLECRU-UHFFFAOYSA-N

애플리케이션

Isopropyl p-toluenesulfonate can be used as a reactant:
  • For the alkylation of amines in the presence of triethylamine.
  • For the O-alkylation of cyclic thiohydroxamic acids in the presence of tetrabutylammonium hydroxide.
  • To synthesize 3-methyl-2-phenyl-1-butanol by reacting with styrene in the presence of bromo(2-cyclohexylethyl)magnesium and zirconocene dichloride.
Isopropyl p-toluenesulfonate can be used:
  • as a thermal acid generator that synthesizes inherently stretchable p-conjugated polymer
  • as a catalyst for the deprotection of PBHEMA [Poly(2-(tert-butoxycarbonyloxy)ethyl methacrylate)] on heating

픽토그램

Exclamation mark
GHS07

신호어

Warning

유해 및 위험 성명서

H315,H319,H335

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)

Not applicable

Flash Point (°C)

Not applicable

가장 최신 버전 중 하나를 선택하세요:

시험 성적서(COA)

Lot/Batch Number
BGBC5662V
BGBC5661V
BGBC4527V
BGBC3245V
MKBR1442V

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Design, Synthesis and Antimicrobial Evaluation of Novel Tricyclic Benzoxazine Fluoroquinolones under Conventional and Microwave Methods
Guruswamy B, et al.
Journal of Heterocyclic Chemistry, 52, 532-538 (2015)
B Y P Tay et al.
International journal of cosmetic science, 38(6), 627-633 (2016-05-14)
Isopropyl p-toluenesulfonate (IPTS) is a potentially genotoxic by-product formed during the esterification of palm oil-based palmitic and palm kernel oil-based myristic acid with isopropanol to produce isopropyl palmitate or isopropyl myristate. There are no methods described for the analysis of
J de Armas et al.
Organic letters, 3(13), 2097-2100 (2001-06-22)
[reaction: see structure] The first examples of efficient electrophilic Zr-catalyzed carbomagnesations are disclosed, where in contrast to previous catalytic carbomagnesations the alkyl moiety of the electrophile is transferred (vs that of the Grignard reagent). The identity of the Grignard reagent
Satsuki Chikura et al.
Mutation research, 811, 110-116 (2016-12-10)
As part of a collaborative study in the Mammalian Mutagenicity Study group of the Japanese Environmental Mutagen Society, we evaluated the in vivo mutagenicity of isopropyl p-toluenesulfonate (IPTS) using a peripheral blood Pig-a assay in rats. Pig-a mutant frequency (MF)

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