5-METHOXY-2-METHYLINDOLE

5-METHOXY-2-METHYLINDOLE Structure
CAS No.
1076-74-0
Chemical Name:
5-METHOXY-2-METHYLINDOLE
Synonyms
NSC 63817;AKOS JY2082626;5-Methoxy-2-methyindole;2-Methyl-5-Methoxyindole;5-METHOXY-2-METHYLINDOLE;Indole, 5-methoxy-2-methyl-;5-Methoxy-2-methylindole>5-Methoxy-2-methylindole 99%;1H-Indole, 5-methoxy-2-methyl-;5-Methoxy-2-methylindole, 99+%
CBNumber:
CB8174569
Molecular Formula:
C10H11NO
Molecular Weight:
161.2
MOL File:
1076-74-0.mol
MSDS File:
SDS
Modify Date:
2024/7/7 20:48:41

5-METHOXY-2-METHYLINDOLE Properties

Melting point 86-88 °C (lit.)
Boiling point 145 °C / 1.5mmHg
Density 1.0840 (rough estimate)
refractive index 1.5200 (estimate)
storage temp. Keep in dark place,Sealed in dry,Room Temperature
solubility Soluble in methanol (very faint turbidity.)
pka 17.28±0.30(Predicted)
form Crystalline Powder or Crystals
color White to light beige
InChIKey VSWGLJOQFUMFOQ-UHFFFAOYSA-N
CAS DataBase Reference 1076-74-0(CAS DataBase Reference)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H332-H335
Precautionary statements  P261-P280-P305+P351+P338
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  37/39-26
WGK Germany  3
HazardClass  IRRITANT
HS Code  29339900
NFPA 704
1
2 0

5-METHOXY-2-METHYLINDOLE price More Price(4)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) M15451 5-Methoxy-2-methylindole 99% 1076-74-0 1G ₹5769.73 2022-06-14 Buy
Sigma-Aldrich(India) M15451 5-Methoxy-2-methylindole 99% 1076-74-0 5G ₹18683.95 2022-06-14 Buy
TCI Chemicals (India) M0730 5-Methoxy-2-methylindole min. 99.0 % 1076-74-0 1G ₹5400 2022-05-26 Buy
TCI Chemicals (India) M0730 5-Methoxy-2-methylindole min. 99.0 % 1076-74-0 5G ₹22800 2022-05-26 Buy
Product number Packaging Price Buy
M15451 1G ₹5769.73 Buy
M15451 5G ₹18683.95 Buy
M0730 1G ₹5400 Buy
M0730 5G ₹22800 Buy

5-METHOXY-2-METHYLINDOLE Chemical Properties,Uses,Production

Description

5-methoxy-2-methylindole is a useful organic raw material. It can be used as the reactant in the preparation of indolylquinoxalines by condensation reactions, in preparation of alkylindoles via Ir-catalyzed reductive alkylation, in arylation reactions in the presence of a palladium acetate catalyst, in enantioselective Friedel-Crafts alkylation, as well as in stereo selective synthesis of cyclopentaindolones via stereoselective [3+2] cyclopentannulation. It is also employed in inhibiting the chlorinating activity of myeloperoxidase (MPO) and in the metabolic synthesis of acrylacetic acid anti-inflammatory synthesis.

Chemical Properties

white to light beige crystalline powder or

Uses

An indole derivative shown to be an effective inhibitor of the chlorinating activity of myeloperoxidase (MPO). Used in the metabolic synthesis of arylacetic acid antiinflammatory synthesis.

References

https://www.alfa.com/en/catalog/B21348/
http://www.sigmaaldrich.com/catalog/product/aldrich/m15451?lang=en&region=US
https://pubchem.ncbi.nlm.nih.gov/compound/5-Methoxy-2-methylindole#section=2D-Structure

Global( 219)Suppliers
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5-Methoxy-2-methylindole, 99+% 5-METHOXY-2-METHYLINDOLE AKOS JY2082626 5-Methoxy-2-methyindole Indole, 5-methoxy-2-methyl- 5-Methoxy-2-Methylindole, 99+% 25GR 5-Methoxy-2-Methylindole, 99+% 5GR 2-Methyl-5-Methoxyindole NSC 63817 5-Methoxy-2-methylindole 99% 1H-Indole, 5-methoxy-2-methyl- 5-Methoxy-2-methylindole> 5-Methoxy-2-methylindole, 99%, for synthesis 1076-74-0 Heterocyclic Building Blocks Building Blocks Simple Indoles Indoles Building Blocks C10 Chemical Synthesis Heterocyclic Building Blocks Aromatics Heterocycles Inhibitors Intermediates & Fine Chemicals Pharmaceuticals Indoles Simple Indoles Building Blocks Heterocyclic Building Blocks Indole Indoles and derivatives