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Bemotrizinol

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Identification
Molecular formula
C38H49N3O5
CAS number
187393-00-6
IUPAC name
[3-(methoxycarbonylamino)phenyl] N-(m-tolyl)carbamate
State
State

At room temperature, Bemotrizinol is in a solid state.

Melting point (Celsius)
128.00
Melting point (Kelvin)
401.00
Boiling point (Celsius)
380.00
Boiling point (Kelvin)
653.00
General information
Molecular weight
628.05g/mol
Molar mass
628.0530g/mol
Density
1.2500g/cm3
Appearence

Bemotrizinol is a yellowish crystalline powder.

Comment on solubility

Solubility of [3-(methoxycarbonylamino)phenyl] N-(m-tolyl)carbamate

The solubility of [3-(methoxycarbonylamino)phenyl] N-(m-tolyl)carbamate in various solvents is a significant consideration in its application and utilization. While specific solubility data might not be extensive, several general principles can be applied:

  • Polar vs. Non-Polar Solvents: Compounds with polar functional groups, like the amine and carbamate functionalities in this molecule, tend to have better solubility in polar solvents such as water or methanol.
  • Hydrogen Bonding: The presence of hydrogen bond donors and acceptors in the structure can enhance solubility. In this case, the –NH and –COO groups may contribute positively to solubility in polar environments.
  • Temperature Effect: Generally, increasing temperature can increase the solubility of many compounds. It can be useful to consider if heating a solvent could help dissolve this compound.
  • pH Sensitivity: The solubility might also be pH-dependent, as ionization of the functional groups can change with the acidity or basicity of the solution.

In conclusion, understanding the solubility of [3-(methoxycarbonylamino)phenyl] N-(m-tolyl)carbamate requires considering these factors, especially its polar characteristics, which likely enhance its solubility in polar solvents.

Interesting facts

Interesting Facts about [3-(methoxycarbonylamino)phenyl] N-(m-tolyl)carbamate

[3-(methoxycarbonylamino)phenyl] N-(m-tolyl)carbamate is a fascinating compound that falls within the category of carbamates, which are recognized for their diverse applications in various fields, including pharmaceuticals and agriculture. Here are some noteworthy details:

  • Structural Diversity: This compound features a unique combination of a methoxycarbonylamino group and a m-tolyl moiety. The presence of these functional groups contributes to its distinctive chemical properties, making it an interesting subject for study in organic chemistry.
  • Potential Applications: Due to the presence of the carbamate functional group, this compound has the potential for use in the synthesis of bioactive molecules. Carbamates have been thoroughly studied for their role as insecticides, herbicides, and even in developing certain pharmaceuticals.
  • Synthesis Techniques: The synthesis of compounds like this often involves various organic reactions, including amine coupling and carbonyl chemistry. These techniques can provide insights into reaction mechanisms and help in understanding the behavior of reactive intermediates.
  • Biological Activity: Certain carbamate derivatives have been noted for their herbicidal properties, drawing interest from the agricultural sector. Thus, studying this compound could help uncover both beneficial and detrimental biological interactions.
  • Research Implications: Given its intriguing structure, researchers are encouraged to explore the reactivity and stability of this compound, as these properties could reveal important information about its potential uses and applications.

In summary, the study of [3-(methoxycarbonylamino)phenyl] N-(m-tolyl)carbamate is not only intellectually stimulating due to its chemical composition but also bears the potential for practical applications across multiple domains. As one researcher put it, "Every compound has a story – it’s our job to understand it."

Synonyms
Phenmedipham
13684-63-4
BETANAL
Phenmedipham [ISO]
Phenmediphame [ISO-French]
Methyl 3-(3-methylcarbaniloyloxy)carbanilate
Beetomax
Betosip
CCRIS 6091
Alegro
Beetup
Fender
Gusto
Phenmedipham [ANSI:BSI:ISO]
Tripart beta
HSDB 1402
Betanal E
Protrum K
Kemifam FL
UNII-UJE31KXP78
EINECS 237-199-0
EPA Pesticide Chemical Code 098701
BRN 2395027
Betamix (Salt/Mix)
DTXSID1024255
Medipham (Salt/Mix)
CHEBI:81734
PHENMEDIPHAM [MI]
Synbetan mix (Salt/Mix)
Betanal tandem (Salt/Mix)
PHENMEDIPHAM [HSDB]
Betanal compact (Salt/Mix)
DTXCID304255
3-[(Methoxycarbonyl)amino]phenyl N-(3-methylphenyl)carbamate
Carbanilic acid, m-hydroxy-, methyl ester, m-methylcarbanilate (ester)
Ethofumesate-phenmedipham (Salt/Mix)
3-(methoxyformamido)phenyl (3-methylphenyl)carbamate
SN 38584
Methyl m-hydroxycarbanilate m-methylcarbanilate
3-methoxycarbonyl-N-(3'-methylphenyl)-carbamate
Phenmediphame (ISO-French)
METHYL-M-HYDROXYCARBANILATE-M-METHYLCARBANILATE
Phenmedipham (ANSI:BSI:ISO)
3-((METHOXYCARBONYL)AMINO)PHENYL N-(3-METHYLPHENYL)CARBAMATE
Phendipham
Betaflow
Betalion
Medipham
Spinaid
Vanguard
Pistol
Suplex
Headland dephend
Tripart beta 2
1-3-((hydroxy(methoxy)methylidene)amino)phenoxy-N-(3-methylphenyl)methanimidic acid
1-3-{[hydroxy(methoxy)methylidene]amino}phenoxy-N-(3-methylphenyl)methanimidic acid
STEPHAM
Schering38584
Pistol 400
Ethofumesate-phenmedipham
EP452
Methyl3mtolycarbamoloxyphenyl carbamate
SN38584
3MethoxycarbonylN(3'methylphenyl)carbamat
Methanol, 1-(3-(((1E)-hydroxymethoxymethylene)amino)phenoxy)-1-((3-methylphenyl)imino)-, (E)-
Methyl 3(3methylcarbaniloyloxy)carbanilate
Methyl3hydroxycarbanilate3methylcarbanilate
Methyl 3(mtolylcarbamoyloxy)phenylcarbamate
3(Carbomethoxyamino)phenyl 3methylcarbanilate
Methyl mhydroxycarbanilate, mmethylcarbanilate
3Methoxycarbonylaminophenyl 3'methylcarbanilate
Methyl-3-(3-methylcarbaniloyloxy) carbanilate
3Methoxycarbonylaminophenyl N3'methylphenylcarbamate
METHYL 3-(M-TOYLCARBAMOYLOXY)PHENYLCARBAMATE
Methyl mhydroxycarbanilate mmethylcarbanilate (ester)
mHydroxycarbanilic acid methyl ester mmethylcarbanilate
3((Methoxycarbonyl)amino)phenyl (3methylphenyl)carbamate
Methyl N(3(N(3methylphenyl)carbamoyloxy)phenyl)carbamate
Methyl mhydroxycarbanilate mmethylcarbanilate (ester) (8CI)
phenmedipham (ISO);methyl 3-(3-methylcarbaniloyloxy)carbanilate
3(Methylphenyl)carbamic acid 3((methoxycarbonyl)amino)phenyl ester
Carbanilic acid, mhydroxy, methyl ester, mmethylcarbanilate (ester)
M-HYDROXYCARBANILIC ACID, METHYL ESTER, M-METHYLCARBANILATE
Carbamic acid, (3methylphenyl), 3((methoxycarbonyl)amino)phenyl ester
CARBANILIC ACID, M-METHYL-, ESTER WITH METHYL M-HYDROXYCARBANILATE
3-(METHYLPHENYL) CARBAMIC ACID 3-((METHOXYCARBONYL)AMINO) PHENYL ESTER
237-199-0
idowtholjbtafi-uhfffaoysa-n
3-((Methoxycarbonyl)amino)phenyl m-tolylcarbamate
Fenmedifam
Spin-aid
Phenmediphame
Kemifam
Synbetan P
Schering 4072
Schering-38584
[3-(methoxycarbonylamino)phenyl] N-(3-methylphenyl)carbamate
EP-452
SN 4075
SN-38584
Methyl 3-(m-tolylcarbamoyloxy)phenylcarbamate
3-((Methoxycarbonyl)amino)phenyl (3-methylphenyl)carbamate
3-(Carbomethoxyamino)phenyl 3-methylcarbanilate
UJE31KXP78
Carbamic acid, (3-methylphenyl)-, 3-((methoxycarbonyl)amino)phenyl ester
3-Methoxycarbonylaminophenyl N-3'-methylphenylcarbamate
m-Hydroxycarbanilic acid methyl ester m-methylcarbanilate
3-[(Methoxycarbonyl)amino]phenyl (3-methylphenyl)carbamate
CHEMBL1079421
3-Methoxycarbonyl-N-(3'-methylphenyl)-carbamat
3-(Methylphenyl)carbamic acid 3-((methoxycarbonyl)amino)phenyl ester
Carbamic acid, (3-methylphenyl)-, 3-[(methoxycarbonyl)amino]phenyl ester
Carbanilic acid, m-hydroxy-, methyl ester, m-methylcarbanilate
Methyl N-(3-(N-(3-methylphenyl)carbamoyloxy)phenyl)carbamate
Caswell No. 648B
Morton EP 452
3-((Methoxycarbonyl)amino)phenyl N-(3-methylphenyl)carbamate (Phenmedipham)
CAS-13684-63-4
Methyl N-[3-[N-(3-methylphenyl)carbamoyloxy]phenyl]carbamate
Methyl-3-m-tolycarbamoloxyphenyl carbamate
Methyl-3-hydroxycarbanilate-3-methylcarbanilate
Methyl m-hydroxycarbanilate, m-methylcarbanilate
S 4075
3-Methoxycarbonylaminophenyl 3'-methylcarbanilate
3-Methoxycarbonyl-N-(3'-methylphenyl)-carbamat [German]
Carbanilic acid, m-hydroxy, methyl ester, m-methylcarbanilate (ester)
SCHEMBL54580
Methyl m-hydroxycarbanilate m-methylcarbanilate (ester)
HY-B2032
Tox21_201295
Tox21_303044
BDBM50311785
AKOS015895890
DS-2923
NCGC00090870-01
NCGC00090870-02
NCGC00257194-01
NCGC00258847-01
AC-37611
DA-66663
DB-042361
CS-0014127
NS00001690
C18420
Phenmedipham, PESTANAL(R), analytical standard
Q2085502
3-methoxycarbonylaminophenyl N-3'methylphenylcarbamate
Phenmedipham (3-Methoxycarbonylaminophenyl-N-3'-methylphenyl