Conditions | Yield |
---|---|
With sodium carbonate In water at 20℃; for 0.166667h; | 100% |
With sodium hydrogencarbonate In water; ethyl acetate | |
With potassium carbonate In water | 3.63 g |
N,N-dimethyl-1,3-phenylenediamine dihydrochloride
Conditions | Yield |
---|---|
With pyridine In chloroform at -20 - 20℃; | 90% |
3-bromo-8-chloro-imidazo[1,2-a]pyrazine
3,8-dibromo-imidazo[1,2-a]pyrazine
N,N-dimethyl-1,3-phenylenediamine dihydrochloride
C14H14BrN5
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine In 1-methyl-pyrrolidin-2-one at 160℃; for 18h; | 77% |
8-chloroimidazo[1,2-α]pyrazine
8-bromoimidazo[1,2-a]pyrazine
N,N-dimethyl-1,3-phenylenediamine dihydrochloride
C14H14BrN5
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine In 1-methyl-pyrrolidin-2-one at 160℃; for 18h; | 77% |
N,N-dimethyl-1,3-phenylenediamine dihydrochloride
diethyl malonate
2,4-dihydroxy-7-(dimethylamino)quinoline
Conditions | Yield |
---|---|
Stage #1: N,N-dimethyl-1,3-phenylenediamine dihydrochloride With sodium hydroxide In water Stage #2: diethyl malonate at 200℃; Dean-Stark; | 75% |
N,N-dimethyl-1,3-phenylenediamine dihydrochloride
diethyl malonate
7-(dimethylamino)-4-hydroxyquinolin-2(1H)-one
Conditions | Yield |
---|---|
Stage #1: N,N-dimethyl-1,3-phenylenediamine dihydrochloride With potassium carbonate In water pH=9 - 10; Stage #2: diethyl malonate In diphenylether Sealed tube; Heating; | 74% |
tert-Butoxybis(dimethylamino)methane
N,N-dimethyl-1,3-phenylenediamine dihydrochloride
Conditions | Yield |
---|---|
Stage #1: tert-Butoxybis(dimethylamino)methane; ethyl 2-(2-ethoxy-2-oxoethyl)-4,5-dimethoxybenzoate at 100℃; for 3h; Stage #2: N,N-dimethyl-1,3-phenylenediamine dihydrochloride With acetic acid at 20℃; for 2h; Stage #3: With sodium hydroxide In ethanol at 80℃; for 1h; | 70% |
N,N-dimethyl-1,3-phenylenediamine dihydrochloride
N-[(3RS)-1-(3-azabicyclo[3.2.2]non-3-yl)carbonylmethyl-5,9-dimethyl-2,3-dihydro-2-oxo-1H-1,4-benzodiazepin-3-yl]-N'-[3-(N,N-dimethyl amino)phenyl]urea hydrochloride
Conditions | Yield |
---|---|
With triethylamine In 1,4-dioxane; water; ethyl acetate; N,N-dimethyl-formamide | 67.1% |
Conditions | Yield |
---|---|
Stage #1: N,N-dimethyl-1,3-phenylenediamine dihydrochloride With potassium carbonate In water for 2h; Stage #2: N,N-Dimethylcarbamoyl chloride With triethylamine In dichloromethane at 0 - 20℃; Schotten-Baumann Reaction; Inert atmosphere; | 67% |
N,N-dimethyl-1,3-phenylenediamine dihydrochloride
3,5-ditrifluoromethylisocyanate
1-(3,5-bis(trifluoromethyl)phenyl)-3-((3-dimethylamino)phenyl)urea
Conditions | Yield |
---|---|
Stage #1: N,N-dimethyl-1,3-phenylenediamine dihydrochloride With sodium hydroxide In dichloromethane; water Stage #2: 3,5-ditrifluoromethylisocyanate In dichloromethane at 20℃; for 12h; | 66% |
but-2-ynoic acid [3-cyano-4-(dimethylamino-methyleneamino)-phenyl]-amide
N,N-dimethyl-1,3-phenylenediamine dihydrochloride
Conditions | Yield |
---|---|
With potassium carbonate In acetic acid; acetonitrile for 1h; Heating / reflux; | 58% |
N,N-dimethyl-1,3-phenylenediamine dihydrochloride
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine In isopropyl alcohol at 100℃; for 6h; Microwave irradiation; Inert atmosphere; | 56% |
N,N-dimethyl-1,3-phenylenediamine dihydrochloride
2,4-dioxo-5-N-(2-fluorophenyl)-1-N-(3-methylbut-1-yl)-3-(phenyloxycarbonylamino)-2,3,4,5-tetrahydro-1H-1,5-benzodiazepine
Conditions | Yield |
---|---|
With triethylamine In N,N-dimethyl-formamide at 160℃; for 2h; Condensation; | 50% |
2-chloro-5-nitrobenzoylchloride
N,N-dimethyl-1,3-phenylenediamine dihydrochloride
sodium hydrogencarbonate
N-(3-Dimethylamino)phenyl-(2-chloro-5-nitrophenyl)carboxamide
Conditions | Yield |
---|---|
With pyridine In tetrahydrofuran; ethyl acetate | 49% |
N,N-dimethyl-1,3-phenylenediamine dihydrochloride
glycerol
N,N-dimethylquinolin-7-amine
Conditions | Yield |
---|---|
Stage #1: N,N-dimethyl-1,3-phenylenediamine dihydrochloride With sodium hydroxide In water Stage #2: glycerol With sulfuric acid; sodium iodide at 140 - 150℃; for 3h; Skraup Quinoline Synthesis; Cooling with ice; | 47% |
1-(2-toluoylmethyl)-2-oxo-3-amino-5-pivaloyl-1,3,4,5-tetrahydro-2H-1,5-benzodiazepine
N,N-dimethyl-1,3-phenylenediamine dihydrochloride
1,1'-carbonyldiimidazole
1-[1-(2-toluoylmethyl)-2-oxo-5-pivaloyl-1,3,4,5-tetrahydro-2H-1,5-benzodiazepin-3-yl]-3-[3-(N,N-dimethylamino)phenyl]urea
Conditions | Yield |
---|---|
With triethylamine In tetrahydrofuran | 40.3% |
4-chloro-6-(methoxymethyl)-2-(3-methylphenyl)pyrimidine
N,N-dimethyl-1,3-phenylenediamine dihydrochloride
4-(4-Dimethylaminoanilino)-6-(methoxymethyl)-2-(3-methylphenyl)pyrimidine
Conditions | Yield |
---|---|
With hydrogenchloride In water | 23% |
N,N-dimethyl-1,3-phenylenediamine dihydrochloride
4-chloro-6,7-dimethoxyquinoline-3-carbonitrile
Conditions | Yield |
---|---|
In 2-ethoxy-ethanol for 3h; Substitution; Heating; | 18% |
2-(2,4-dinitrophenyl)acetyl chloride
N,N-dimethyl-1,3-phenylenediamine dihydrochloride
Conditions | Yield |
---|---|
With sodium hydrogencarbonate; benzene |
3-(p-nitrophenyl)propanoyl chloride
N,N-dimethyl-1,3-phenylenediamine dihydrochloride
Conditions | Yield |
---|---|
With sodium hydrogencarbonate; benzene |
3-(2,4-dinitro-phenyl)-propionyl chloride
N,N-dimethyl-1,3-phenylenediamine dihydrochloride
3-(2,4-dinitro-phenyl)-propionic acid-(3-dimethylamino-anilide)
Conditions | Yield |
---|---|
With sodium hydrogencarbonate; benzene |
potassium cyanate
N,N-dimethyl-1,3-phenylenediamine dihydrochloride
3-ureido-1-dimethylaminobenzene
Conditions | Yield |
---|---|
With sodium hydrogencarbonate; benzene | |
With pyridine; acetone |
Conditions | Yield |
---|---|
With sodium hydrogencarbonate; benzene |
N,N-dimethyl-1,3-phenylenediamine dihydrochloride
4-nitrophenylacetyl chloride
Conditions | Yield |
---|---|
With sodium hydrogencarbonate; benzene |
N,N-dimethyl-1,3-phenylenediamine dihydrochloride
3,5-dinitrobenoyl chloride
3,5-dinitro-benzoic acid-(3-dimethylamino-anilide)
Conditions | Yield |
---|---|
With sodium hydrogencarbonate; benzene |
4-Acetyl-phenyl-diazonium
N,N-dimethyl-1,3-phenylenediamine dihydrochloride
N,N-dimethyl-1,3-phenylenediamine dihydrochloride
4-Hydroxymethyl-benzenediazonium
thiophosgene
N,N-dimethyl-1,3-phenylenediamine dihydrochloride
3-N,N-dimethylaminophenylisothiocyanate
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine In toluene at 75℃; |
N,N-dimethyl-1,3-phenylenediamine dihydrochloride
1-(2-cyclopentylethyl)-2,4-dioxo-5-(2-fluorophenyl)-3-isocyanato-2,3,4,5-tetrahydro-1H-1,5-benzodiazepine
Conditions | Yield |
---|---|
In acetonitrile for 7h; Addition; |
The cas register number of N,N-Dimethyl-1,3-phenylenediamine dihydrochloride is 3575-32-4. It also can be called as N,N-Dimethyl-m-phenylenediamine dihydrochloride and the IUPAC Name about this chemical is 3-N,3-N-dimethylbenzene-1,3-diamine dihydrochloride. It belongs to the following product categories, such as Aromatics Compounds, Aromatics and so on.
Physical properties about N,N-Dimethyl-1,3-phenylenediamine dihydrochloride are: (1)ACD/LogP: 1.05; (2)ACD/LogD (pH 5.5): 0.9; (3)ACD/LogD (pH 7.4): 1.04; (4)ACD/BCF (pH 5.5): 2.64; (5)ACD/BCF (pH 7.4): 3.65; (6)ACD/KOC (pH 5.5): 63.51; (7)ACD/KOC (pH 7.4): 87.81; (8)#H bond acceptors: 2; (9)#H bond donors: 2; (10)#Freely Rotating Bonds: 2; (11)Polar Surface Area: 6.48Å2; (12)Flash Point: 88.8 °C; (13)Enthalpy of Vaporization: 48.11 kJ/mol; (14)Boiling Point: 244.1 °C at 760 mmHg; (15)Vapour Pressure: 0.0309 mmHg at 25°C.
When you are using this chemical, please be cautious about it as the following:
This chemical is toxic by inhalation, in contact with skin and if swallowed and it is irritating to eyes, respiratory system and skin, it also may cause sensitization by skin contact. When you are using it, wear suitable protective clothing, gloves and eye/face protection. In case of contact with eyes, rinse immediately with plenty of water and seek medical advice and in case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.)
You can still convert the following datas into molecular structure:
(1)Canonical SMILES: CN(C)C1=CC=CC(=C1)N.Cl.Cl
(2)InChI: InChI=1S/C8H12N2.2ClH/c1-10(2)8-5-3-4-7(9)6-8;;/h3-6H,9H2,1-2H3;2*1H
(3)InChIKey: BZJPIQKDEGXVFG-UHFFFAOYSA-N
About|Contact|Cas|Product Name|Molecular|Country|Encyclopedia
Message|New Cas|MSDS|Service|Advertisement|CAS DataBase|Article Data|Manufacturers | Chemical Catalog
©2008 LookChem.com,License: ICP
NO.:Zhejiang16009103
complaints:service@lookchem.com Desktop View