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Merck

65369

Supelco

(S)-(-)-α-甲氧基-α-三氟甲基苯乙酸

for chiral derivatization, LiChropur, ≥99.0%

别名:

(-)-MTPA, Mosher 酸

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About This Item

经验公式(希尔记法):
C10H9F3O3
CAS号:
分子量:
234.17
Beilstein:
4684048
EC號碼:
MDL號碼:
分類程式碼代碼:
12000000
PubChem物質ID:
NACRES:
NA.22

等級

for chiral derivatization

品質等級

化驗

≥99.0% (T)
≥99.0%

形狀

solid

光學活性

[α]20/D −73±1°, c = 2% in methanol

光學純度

enantiomeric ratio: ≥99.5:0.5 (GC)

品質

LiChropur

技術

HPLC: suitable

bp

90 °C/0.1 mmHg

mp

46-49 °C (lit.)

儲存溫度

2-8°C

SMILES 字串

CO[C@](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)/t9-/m0/s1

InChI 密鑰

JJYKJUXBWFATTE-VIFPVBQESA-N

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應用

Determination of absolute configuration of stereogenic carbinol carbons; doi:10.1038/nprot.2007.354

推薦產品

Discover LiChropur reagents ideal for HPLC or LC-MS analysis

法律資訊

LiChropur is a trademark of Merck KGaA, Darmstadt, Germany

象形圖

Exclamation mark

訊號詞

Warning

危險聲明

危險分類

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

標靶器官

Respiratory system

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

235.4 °F - closed cup

閃點(°C)

113 °C - closed cup

個人防護裝備

dust mask type N95 (US), Eyeshields, Gloves


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分析证书(COA)

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Thomas R Hoye et al.
Organic letters, 12(8), 1768-1771 (2010-03-27)
The relative magnitudes of the chemical shift differences (Deltadeltas) in the two diastereomers of menthyl esters of known chiral derivatizing agents (CDAs) were compared to those of the alpha-methoxy-alpha-trifluoromethyl-1-naphthylacetyl (MTN((1))A) analogues I. Discrimination of the terminal diastereotopic methyl resonances in
Hiroshi Hasegawa et al.
Journal of mass spectrometry : JMS, 46(5), 502-507 (2011-04-19)
D-Serine is a co-agonist of the N-methyl-D-aspartate receptor in glutamate neurotransmission and has been proposed as a potential therapeutic agent for schizophrenia. However, D-serine also acts as a nephrotoxic substance in rats at high doses. To investigate the pharmacokinetics and
Giancarlo Cravotto et al.
Chirality, 16(8), 526-533 (2004-08-04)
Cyclodextrin (CD) derivatives are important selectors for analytical chiral recognition. Their enantioselectivities and chemical properties depend on ring size and on nature, number and location of substituents. This paper describes the synthesis of 6-O-TBDMS-2,3-O-methyl beta-cyclodextrins bearing in position 2 either
Barry J Everitt et al.
Nature neuroscience, 8(11), 1481-1489 (2005-10-28)
Drug addiction is increasingly viewed as the endpoint of a series of transitions from initial drug use--when a drug is voluntarily taken because it has reinforcing, often hedonic, effects--through loss of control over this behavior, such that it becomes habitual
J Martín Torres-Valencia et al.
Phytochemical analysis : PCA, 13(6), 329-332 (2002-12-24)
A method to determine the absolute configuration of 2,3-epoxy-2-methylbutanoate ester residues in natural products is presented, based on (i) the reduction of the ester function to yield a 2-methyl-1,2-butanediol, (ii) esterification of the obtained primary alcohol with either (R)-(+)- or

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