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Merck
CN

I1000

Indole-3-acetaldehyde–sodium bisulfite addition compound

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About This Item

Linear Formula:
C10H9NO · NaHSO3
CAS Number:
Molecular Weight:
263.25
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
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InChI

1S/C10H11NO4S.Na/c12-10(16(13,14)15)5-7-6-11-9-4-2-1-3-8(7)9;/h1-4,6,10-12H,5H2,(H,13,14,15);/q;+1/p-1

SMILES string

[Na].OC(Cc1c[nH]c2ccccc12)S(O)(=O)=O

InChI key

WYKPCRCESPDDQX-UHFFFAOYSA-M

impurities

≤15% excess sodium bisulfite

storage temp.

2-8°C

Quality Level

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Application

  • Reactant for preparation of potential neurotransmitter analogs
  • Reactant for Strecker reaction with cyanide-11C

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


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Hayes, R. L.; et al.
The International Journal of Applied Radiation and Isotopes, 29, 186-186 (1978)
Schlecht, M., F.; Giandinoto, S.
Heterocycles, 25, 485-485 (1987)
Davide Marangon et al.
Glia, 68(10), 2001-2014 (2020-03-13)
In the last decade, microRNAs have been increasingly recognized as key modulators of glial development. Recently, we identified miR-125a-3p as a new player in oligodendrocyte physiology, regulating in vitro differentiation of oligodendrocyte precursor cells (OPCs). Here, we show that miR-125a-3p

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