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Dokumente

156558

Sigma-Aldrich

α-Methoxy-α-(trifluormethyl)-phenylessigsäure

97%

Synonym(e):

MTPA

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About This Item

Lineare Formel:
C6H5C(OCH3)(CF3)CO2H
CAS-Nummer:
56135-03-6
Molekulargewicht:
234.17
MDL-Nummer:
MFCD00066637
UNSPSC-Code:
12352100
PubChem Substanz-ID:
24849618
NACRES:
NA.22

Assay

97%

Brechungsindex

n20/D 1.476 (lit.)

bp

95-98 °C/0.05 mmHg (lit.)

mp (Schmelzpunkt)

41-46 °C (lit.)

Lagertemp.

2-8°C

SMILES String

COC(C(O)=O)(c1ccccc1)C(F)(F)F

InChI

1S/C10H9F3O3/c1-16-9(8(14)15,10(11,12)13)7-5-3-2-4-6-7/h2-6H,1H3,(H,14,15)

InChIKey

JJYKJUXBWFATTE-UHFFFAOYSA-N

Anwendung

Diastereomeric bis-esters of (±)-trans-7,8-dihydroxy-7,8,9,10-tetrahydrobenzo[α]pyrene with MTPA has been used as a noncarcinogenic precursor to obtain the (+)and (-)-dihydrodiols by chromatographic resolution. It has also been used to develop empirically derived correlation of configuration and nmr chemical shifts for diastereomeric MTPA esters.

Piktogramme

Exclamation mark
GHS07

Signalwort

Warning

Gefahreneinstufungen

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

Zielorgane

Respiratory system

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

235.4 °F - closed cup

Flammpunkt (°C)

113 °C - closed cup

Persönliche Schutzausrüstung

dust mask type N95 (US), Eyeshields, Gloves

Analysenzertifikate (COA)

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Nuclear Magnetic Resonance Enantiomer Reagents. Configurational Correlations via Nuclear Magnetic Resonance Chemical Shifts of Diastereomeric Mandelate, 0-Methylmandelate, and α-Methoxy-α-trifluoromethylphenylacetate (MTPA) Esters
Dale JA and Mosher HS
Journal of the American Chemical Society, 95(2), 512-519 (1973)
Yuka Uemura et al.
Chemical & pharmaceutical bulletin, 63(8), 608-616 (2015-08-04)
From the leaves of Meliosma lepidota ssp. squamulata, megastigmane glucosides with spiro-structures and megastigmanes were isolated. Their structures were determined by X-ray crystallographic analyses and spectroscopic investigation. The absolute structures of the megastigmanes were determined by the modified Mosher's method.
W Levin et al.
The Journal of biological chemistry, 255(19), 9067-9074 (1980-10-10)
The (+)- and (-)-enantiomers of benzo[a]pyrene 7,8-oxide are hydrated stereospecifically at C-8 to (-)- and (+)-trans-7,8-dihydroxy-7,8-dihydrobenzo[a]pyrene, respectively, by rat hepatic epoxide hydrolase. The (-)-enantiomer of benzo[a]pyrene 7,8-oxide is metabolized by microsomal epoxide hydrolase at a rate 3- to 4-fold greater
Dongsheng Du et al.
Fitoterapia, 101, 73-79 (2015-01-07)
Two new germacrane sesquiterpenes, yedoensins A (1) and B (2), together with 8 known ones (3-10) were isolated from the herb of Viola yedoensis. The structures of the new compounds were established by extensive spectroscopic means including 1D ((1)H and
Guangyu Wang et al.
Oncology letters, 10(5), 2835-2841 (2016-01-02)
MicroRNA-181 (miR-181) has been recently demonstrated to participate in the differentiation and development of immune cells, including natural killer cells and B and T lymphocytes, and myeloid linages, including erythroid and megakaryocytic cells. The aberrant expression of miR-181, particularly low
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