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Merck
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文件

576662

Sigma-Aldrich

吲哚-6-羧酸

97%

同義詞:

6-Carboxyindole

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About This Item

經驗公式(希爾表示法):
C9H7NO2
CAS號碼:
分子量::
161.16
Beilstein:
123991
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

化驗

97%

mp

249-253 °C (lit.)

SMILES 字串

OC(=O)c1ccc2cc[nH]c2c1

InChI

1S/C9H7NO2/c11-9(12)7-2-1-6-3-4-10-8(6)5-7/h1-5,10H,(H,11,12)

InChI 密鑰

GHTDODSYDCPOCW-UHFFFAOYSA-N

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應用

  • Reactant for preparation of D-glutamic acid-based inhibitors of E. coli MurD ligase
  • Reactant for preparation of indolylindazoles and indolylpyrazolopyridines as interleukin-2 inducible T cell kinase inhibitors
  • Reactant for preparation of amide conjugates with ketoprofen, as inhibitors of Gli1-mediated transcription in Hedgehog pathway
  • Reactant for preparation of piperazine-bisamide analogs as human growth hormone secretagogue receptor antagonists for treatment of obesity
  • Reactant for preparation of pyridinyl carboxylates via esterification with chlorohydroxypyridine as SARS-CoV 3CL proinhibitors
  • Reactant for preparation of (indolecarbonyl)-D-phenylglycinamide amides as factor Xa inhibitors

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

Eyeshields, Gloves, type N95 (US)


分析證明 (COA)

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Thomas Heine et al.
Applied biochemistry and biotechnology, 181(4), 1590-1610 (2016-11-11)
The enantioselective epoxidation of styrene and related compounds by two-component styrene monooxygenases (SMOs) has targeted these enzymes for development as biocatalysts. In the present work, we prepare genetically engineered fusion proteins that join the C-terminus of the epoxidase (StyA) to

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