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(3,6-dihydroxy-1-methyl-indolin-5-yl)iminourea

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Identification
Molecular formula
C10H13N3O3
CAS number
Not Available
IUPAC name
(3,6-dihydroxy-1-methyl-indolin-5-yl)iminourea
State
State

At room temperature, this compound is typically a solid. It has a stable crystalline form that does not readily evaporate or change state at standard conditions.

Melting point (Celsius)
243.00
Melting point (Kelvin)
516.15
Boiling point (Celsius)
400.00
Boiling point (Kelvin)
673.15
General information
Molecular weight
235.25g/mol
Molar mass
235.2530g/mol
Density
1.3900g/cm3
Appearence

The compound typically presents as a solid at room temperature with a crystalline structure. The color may range from off-white to slightly yellow, depending on purity and specific form.

Comment on solubility

Solubility of (3,6-dihydroxy-1-methyl-indolin-5-yl)iminourea

The solubility of (3,6-dihydroxy-1-methyl-indolin-5-yl)iminourea (C10H13N3O3) can be influenced by several factors, making its behavior in various solvents a subject of interest. Here’s a synthesis of notable considerations:

  • Polarity: The presence of multiple hydroxyl (-OH) groups in this compound increases its polarity, which generally enhances solubility in polar solvents such as water.
  • Hydrogen Bonding: Strong hydrogen bonding capability due to hydroxyl and amine groups can lead to significant solubility in aqueous solutions.
  • Solvent Effects: It is expected to have limited solubility in nonpolar solvents (e.g., hexane, benzene), as polar compounds tend to interact poorly with nonpolar molecules.
  • pH Influence: The solubility may also vary with pH; acidic or basic conditions could facilitate protonation or deprotonation, further affecting its solubility behavior.

In summary, while (3,6-dihydroxy-1-methyl-indolin-5-yl)iminourea is likely to be soluble in polar solvents, particularly water, its solubility in organic solvents depends on the specific conditions and the solvent's polarity. Such understanding can be critical for applications in pharmaceuticals or material sciences.

Interesting facts

Interesting Facts about (3,6-Dihydroxy-1-methyl-indolin-5-yl)iminourea

(3,6-Dihydroxy-1-methyl-indolin-5-yl)iminourea is a fascinating compound that combines elements from various branches of organic chemistry. Here are some compelling insights:

  • Structural Diversity: This compound features an indole framework, which is a bicyclic structure that is widely found in many natural products and pharmaceuticals. The presence of two hydroxyl groups at the 3 and 6 positions adds to its reactivity and versatility in synthesis.
  • Biological Activity: Compounds similar to this one are often investigated for their potential biological activities. The indole structure is known for its role in various biological processes, including neurotransmission, and may influence pharmacological properties.
  • Derivative Potential: The amine functional group from the iminourea moiety opens up a range of possibilities for further chemical modifications. This could lead to the development of new derivatives with enhanced properties or selectivity in biological systems.
  • Applications in Research: Researchers may utilize this compound in various fields, especially in drug discovery and development. Understanding how substituents affect activity can lead to innovative therapeutic agents.
  • Literary Presence: The indole and imine systems are often referenced in literature due to their intriguing chemistry and utility, making this compound not just a chemical, but a part of scientific stories that illustrate the beauty of organic synthesis.

As we delve into the world of chemistry, compounds like (3,6-dihydroxy-1-methyl-indolin-5-yl)iminourea remind us of the endless possibilities that exist in molecular design and the importance of structure in determining function. Science is truly a journey where chemistry serves as our guide!

Synonyms
carbazochrome
69-81-8
Adrenochrome semicarbazone
Adrenochrome monosemicarbazone
Adedolon
Adrenostazin
Carbazochrom
Adchnon
2-(3-Hydroxy-1-methyl-6-oxo-2,3-dihydro-1H-indol-5(6H)-ylidene)hydrazinecarboxamide
Cromadrenal
Sangostasin
Sangostazin
Adrenoxyl
Adrezon
Adrokson
Adroxon
Cartabes
Adrenostan
Cromosil
Carbazocromo
Adenocrome monosemicarbazone
NSC 73742
(3,6-dihydroxy-1-methyl-2,3-dihydroindol-5-yl)iminourea
3-Hydroxy-1-methyl-5,6-inodlindionsemicarbazon
NSC-73742
DTXSID3048310
81F061RQS4
3-Hydroxy-1-methyl-5,6-indolinedione semicarbazone
MFCD00130253
Hydrazinecarboxamide, 2-(1,2,3,6-tetrahydro-3-hydroxy-1-methyl-6-oxo-5H-indol-5-ylidene)-
NCGC00164521-01
Adrenoxil
Cromoxin
Apara
5,6-INDOLINEDIONE, 3-HYDROXY-1-METHYL-, 5-SEMICARBAZONE
Carbazochromum
Adrenochrome monosemicarbazone; Adrenostazin; Adrenoxyl; Adrezon
Carbazochrome [INN:JAN]
Adrenochrome monosemicarbazon
Carbazochromum [INN-Latin]
Carbazocromo [INN-Spanish]
EINECS 200-717-0
UNII-81F061RQS4
L 502
Carbazochrome,(S)
3-Hydroxy-1-methyl-5-semicarbazono-6(5H)-indolinon
Adrenochromsemicarbazon
Carbazochrome (Standard)
[(Z)-(3-hydroxy-1-methyl-6-oxo-2,3-dihydroindol-5-ylidene)amino]urea
Carbazochrome (JAN/INN)
CARBAZOCHROME [MI]
CARBAZOCHROME [INN]
CARBAZOCHROME [JAN]
CARBAZOCHROME [MART.]
SCHEMBL506178
CARBAZOCHROME [WHO-DD]
CHEMBL2051960
CHEMBL4789892
SCHEMBL11036230
CHEBI:31349
HY-B1587R
DTXCID00809636
SSCSSDNTQJGTJT-UHFFFAOYSA-N
XSXCZNVKFKNLPR-SDQBBNPISA-N
XSXCZNVKFKNLPR-UHFFFAOYSA-N
BCP15360
HY-B1587
NSC73742
Tox21_113160
s5084
ZINC03871875
AKOS015896532
AKOS024319075
AKOS030242682
CCG-266833
DB09012
DS-4533
FA70002
SB67333
CAS-69-81-8
NCGC00344541-01
AC-31089
DA-62054
SY057431
5, 3-hydroxy-1-methyl-, 5-semicarbazone
ADRENOCHROME MONOSEMICARBAZONE [MI]
A0176
CS-0013486
NS00077991
D01864
H11624
6-Indolinone, 3-hydroxy-1-methyl-5-semicarbazono-
Q1104521
5,6-dihydro-3-hydroxy-1-methyl-5,6-indolindion-5-semicarbazon
2,3-Dihydro-3-hydroxy-1-methyl-1H-indole-5,6-dione-5-semicarbazone
3-Hydroxy-1-methyl-2,3-dihydro-1H-indole-5,6-dione 5-semicarbazone #
(E)-2-(3-hydroxy-1-methyl-6-oxo-2,3-dihydro-1H-indol-5(6H)-ylidene)hydrazinecarboxamide
{[(5E)-3-Hydroxy-1-methyl-6-oxo-2,3,5,6-tetrahydro-1H-indol-5-ylidene]amino}urea
Hydrazinecarboxamide,2,3,6-tetrahydro-3-hydroxy-1-methyl-6-oxo-5H-indol-5-ylidene)-