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Merck
CN

50051

Glycine benzyl ester p-toluenesulfonate salt

≥99.0% (T)

Synonym(s):

Benzyl glycinate p-toluenesulfonate salt

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About This Item

Linear Formula:
NH2CH2COOCH2C6H5 · CH3C6H4SO3H
CAS Number:
Molecular Weight:
337.39
UNSPSC Code:
12352209
NACRES:
NA.22
PubChem Substance ID:
EC Number:
217-094-6
Beilstein/REAXYS Number:
3600116
MDL number:
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form

solid

InChI

1S/C9H11NO2.C7H8O3S/c10-6-9(11)12-7-8-4-2-1-3-5-8;1-6-2-4-7(5-3-6)11(8,9)10/h1-5H,6-7,10H2;2-5H,1H3,(H,8,9,10)

InChI key

WJKJXKRHMUXQSL-UHFFFAOYSA-N

SMILES string

Cc1ccc(cc1)S(O)(=O)=O.NCC(=O)OCc2ccccc2

assay

≥99.0% (T)

reaction suitability

reaction type: solution phase peptide synthesis

mp

132-134 °C

solubility

methanol: 0.1 g/mL, clear

application(s)

peptide synthesis

Quality Level

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


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Yang Lin et al.
Molecules (Basel, Switzerland), 25(19) (2020-10-04)
The discovery of IDO1 and HDAC1 dual inhibitors may provide a novel strategy for cancer treatment by taking advantages of both immunotherapeutic and epigenetic drugs. In this paper, saprorthoquinone (1) and 13 of its analogues from Salvia prionitis Hance were

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