ChemicalBook > CAS DataBase List > 7-METHYLINDOLE-3-CARBOXALDEHYDE

7-METHYLINDOLE-3-CARBOXALDEHYDE

Product Name
7-METHYLINDOLE-3-CARBOXALDEHYDE
CAS No.
4771-50-0
Chemical Name
7-METHYLINDOLE-3-CARBOXALDEHYDE
Synonyms
Antifungal agent 98;CCR1/5/8 activator 1;3-FORMYL-7-METHYLINDOLE;7-METHYLINDOLE-3-ALDEHYDE;7-Methyl-3-carboxaldehyde;7-METHYLINDOLE-3-CARBOXALDEHYDE;7-Methyl-3-indolecarboxaldehyde;7-METHYLINDOLE-3-CARBOXYALDEHYDE;7-METHYL-1H-INDOLE-3-CARBALDEHYDE;7-Methylindole-3-carboxaldehyde 98%
CBNumber
CB0229603
Molecular Formula
C10H9NO
Formula Weight
159.18
MOL File
4771-50-0.mol
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7-METHYLINDOLE-3-CARBOXALDEHYDE Property

Melting point:
206-208°C
Boiling point:
341.0±22.0 °C(Predicted)
Density 
1.226±0.06 g/cm3(Predicted)
storage temp. 
Inert atmosphere,Store in freezer, under -20°C
form 
Solid
pka
15.80±0.30(Predicted)
color 
Yellow to brown
Sensitive 
Air Sensitive
BRN 
122340
InChI
InChI=1S/C10H9NO/c1-7-3-2-4-9-8(6-12)5-11-10(7)9/h2-6,11H,1H3
InChIKey
KTUFZHVVJBHGKZ-UHFFFAOYSA-N
SMILES
N1C2=C(C=CC=C2C)C(C=O)=C1
CAS DataBase Reference
4771-50-0(CAS DataBase Reference)
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Safety

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36-37
WGK Germany 
3
Hazard Note 
Irritant
HS Code 
29339900
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P304+P340IF INHALED: Remove victim to fresh air and Keep at rest in a position comfortable for breathing.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

P405Store locked up.

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N-Bromosuccinimide Price

TRC
Product number
M313628
Product name
7-Methylindole-3-carboxyaldehyde
Packaging
100mg
Price
$75
Updated
2021/12/16
Matrix Scientific
Product number
069433
Product name
3-Formyl-7-methylindole
Purity
96%
Packaging
500mg
Price
$57
Updated
2021/12/16
Matrix Scientific
Product number
069433
Product name
3-Formyl-7-methylindole
Purity
96%
Packaging
1g
Price
$72
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
CHM1555378
Product name
7-METHYLINDOLE-3-CARBOXALDEHYDE
Purity
95.00%
Packaging
250MG
Price
$120.82
Updated
2021/12/16
SynQuest Laboratories
Product number
4H15-1-55
Product name
7-Methylindole-3-carboxaldehyde
Purity
98%
Packaging
1g
Price
$176
Updated
2021/12/16
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7-METHYLINDOLE-3-CARBOXALDEHYDE Chemical Properties,Usage,Production

Uses

Reactant for preparation of:• ;Tryptophan dioxygenase inhibitors pyridyl-ethenyl-indoles as potential anticancer immunomodulators1• ;Antibacterial and antituberculosis agents2• ;Antiandrogens effective against androgen receptor mutants3• ;Anti-bovine viral diarrhea virus (BVDV) agents4• ;Receptor subtype 5 antagonists5• ;Glucocorticoid receptor ligands6• ;Necroptosis inhibitors7• ;Orally efficacious small-molecule sctivator of the insulin receptor8

Uses

Reactant for preparation of:

  • Tryptophan dioxygenase inhibitors pyridyl-ethenyl-indoles as potential anticancer immunomodulators
  • Antibacterial and antituberculosis agents
  • Antiandrogens effective against androgen receptor mutants
  • Anti-bovine viral diarrhea virus (BVDV) agents
  • Receptor subtype 5 antagonists
  • Glucocorticoid receptor ligands
  • Necroptosis inhibitors
  • Orally efficacious small-molecule sctivator of the insulin receptor

Synthesis

933-67-5

100-97-0

4771-50-0

General procedure for the synthesis of 7-methylindole-3-carboxaldehyde from 7-methylindole and ouvertropine: To a 50 mL round-bottomed flask fitted with a magnetic stirrer were added sequentially 7-methylindole (1.0 mmol, 1.0 eq.), hexamethylenetetetramine (HMTA, 2.0 mmol, 0.2803 g, 2.0 eq.), activated carbon (0.1 g), and N,N- dimethylformamide (DMF, 2 mL). Iodine (I2, 0.2 mmol, 0.0507 g, 20 mol%) was then added and the flask was assembled with a reflux condenser tube. The reaction mixture was stirred at 120 °C and the progress of the reaction was monitored by thin layer chromatography (TLC). After completion of the reaction, the mixture was cooled to room temperature. The resulting mixture was filtered through a diatomaceous earth pad and the filter cake was washed well with ethyl acetate (EtOAc, 4 x 6 mL). The combined filtrates were washed sequentially with 0.5 M aqueous hydrochloric acid (10 mL), saturated sodium bicarbonate (NaHCO3) solution (10 mL), and saturated sodium chloride (NaCl) solution (10 mL), dried over anhydrous sodium sulfate (Na2SO4) and concentrated under reduced pressure. The crude product was purified by silica gel fast column chromatography, and the target product 7-methylindole-3-carbaldehyde was obtained by using a mixed solvent of hexane and ethyl acetate as eluent.

References

[1] Tetrahedron Letters, 2017, vol. 58, # 30, p. 2877 - 2880
[2] Patent: CN108329249, 2018, A. Location in patent: Paragraph 0041-0044; 0066-0069

7-METHYLINDOLE-3-CARBOXALDEHYDE Preparation Products And Raw materials

Raw materials

Preparation Products

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7-METHYLINDOLE-3-CARBOXALDEHYDE Suppliers

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View Lastest Price from 7-METHYLINDOLE-3-CARBOXALDEHYDE manufacturers

ZHENGZHOU JIUYI TIME NEW MATERIALS CO,.LTD
Product
7-Methyl-1H-indole-3-carbaldehyde 4771-50-0
Price
US $1.60-6.60/kg
Min. Order
1kg
Purity
99%
Supply Ability
100kg
Release date
2025-06-19
Shaanxi Dideu Medichem Co. Ltd
Product
7-Methylindole-3-carboxaldehyde 4771-50-0
Price
US $1.00-1.50/KG
Min. Order
1KG
Purity
99%
Supply Ability
10000KG
Release date
2024-07-17
Zhuozhou Wenxi import and Export Co., Ltd
Product
7-METHYLINDOLE-3-CARBOXALDEHYDE 4771-50-0
Price
US $15.00-10.00/KG
Min. Order
1KG
Purity
99%+ HPLC
Supply Ability
Monthly supply of 1 ton
Release date
2021-08-11

4771-50-0, 7-METHYLINDOLE-3-CARBOXALDEHYDERelated Search:


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  • 7-Methyl-3-carboxaldehyde
  • 1H-Indole-3-carboxaldehyde, 7-methyl-
  • CCR1/5/8 activator 1
  • Antifungal agent 98
  • 4771-50-0
  • ALDEHYDE
  • Building Blocks
  • Heterocyclic Building Blocks
  • Indoles
  • C10-C12
  • Aldehydes
  • Building Blocks
  • C10
  • Carbonyl Compounds
  • Chemical Synthesis
  • Heterocyclic Building Blocks
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  • Building Blocks
  • Heterocyclic Building Blocks
  • Indoles
  • ALDEHYDE
  • Indoles and derivatives
  • Indole
  • Heterocyclic Compounds