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120-07-0 Usage

Chemical Properties

white to Yellowish crystals. Soluble in benzene, ethanol and ether.

Uses

N-Phenyldiethanolamine can be used for hair coloring agents. It can also be used as a resin composition and can be used to produce cured film and semiconductor device.

Preparation

N-Phenyldiethanolamine is obtained by the addition of aniline and ethylene oxide.

Flammability and Explosibility

Notclassified

Check Digit Verification of cas no

The CAS Registry Mumber 120-07-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,2 and 0 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 120-07:
(5*1)+(4*2)+(3*0)+(2*0)+(1*7)=20
20 % 10 = 0
So 120-07-0 is a valid CAS Registry Number.
InChI:InChI=1/C10H15NO2/c12-8-6-11(7-9-13)10-4-2-1-3-5-10/h1-5,12-13H,6-9H2/p+1

120-07-0 Well-known Company Product Price

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  • (Code)Product description
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  • Alfa Aesar

  • (L13931)  N-Phenyldiethanolamine, 97%   

  • 120-07-0

  • 100g

  • 164.0CNY

  • Detail
  • Alfa Aesar

  • (L13931)  N-Phenyldiethanolamine, 97%   

  • 120-07-0

  • 500g

  • 307.0CNY

  • Detail
  • Alfa Aesar

  • (L13931)  N-Phenyldiethanolamine, 97%   

  • 120-07-0

  • 2500g

  • 987.0CNY

  • Detail
  • Aldrich

  • (P22400)  N-Phenyldiethanolamine  97%

  • 120-07-0

  • P22400-250G

  • 308.88CNY

  • Detail
  • Aldrich

  • (P22400)  N-Phenyldiethanolamine  97%

  • 120-07-0

  • P22400-1KG

  • 744.12CNY

  • Detail

120-07-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2'-(Phenylimino)diethanol

1.2 Other means of identification

Product number -
Other names Ethanol, 2,2‘-(phenylimino)bis-

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Intermediates,Processing aids, not otherwise listed
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:120-07-0 SDS

120-07-0Synthetic route

iodobenzene
591-50-4

iodobenzene

2,2'-iminobis[ethanol]
111-42-2

2,2'-iminobis[ethanol]

2,2'-(phenylimino)bis[ethanol]
120-07-0

2,2'-(phenylimino)bis[ethanol]

Conditions
ConditionsYield
With potassium hydroxide In dimethyl sulfoxide at 100℃; for 3h;95%
aniline
62-53-3

aniline

2-chloro-ethanol
107-07-3

2-chloro-ethanol

2,2'-(phenylimino)bis[ethanol]
120-07-0

2,2'-(phenylimino)bis[ethanol]

Conditions
ConditionsYield
With sodium hydroxide at 100℃; for 72h;87%
With calcium carbonate; potassium iodide In water for 8h; Reflux;86%
With calcium carbonate; potassium iodide In water for 8h; Reflux; Inert atmosphere; Schlenk technique;86%
oxirane
75-21-8

oxirane

aniline
62-53-3

aniline

2,2'-(phenylimino)bis[ethanol]
120-07-0

2,2'-(phenylimino)bis[ethanol]

Conditions
ConditionsYield
With water; propionic acid at 0 - 10℃;85%
at 80 - 90℃; im Rohr;
at 80 - 90℃;
[1,3]-dioxolan-2-one
96-49-1

[1,3]-dioxolan-2-one

aniline
62-53-3

aniline

A

2,2'-(phenylimino)bis[ethanol]
120-07-0

2,2'-(phenylimino)bis[ethanol]

B

2-Anilinoethanol
122-98-5

2-Anilinoethanol

Conditions
ConditionsYield
With tri-i-butyl(methyl)phosphonium tosylate at 170℃; for 8h; Ionic liquid; Neat (no solvent);A 74%
B n/a
With Na-Y zeolite In Triethylene glycol dimethyl ether at 160℃; for 2h;A 19%
B 63%
In neat (no solvent) at 140℃; for 14h;
methanol
67-56-1

methanol

formaldehyd
50-00-0

formaldehyd

aniline
62-53-3

aniline

A

2,2'-(phenylimino)bis[ethanol]
120-07-0

2,2'-(phenylimino)bis[ethanol]

B

2-Anilinoethanol
122-98-5

2-Anilinoethanol

Conditions
ConditionsYield
With tert.-butylhydroperoxide; titanium(III) chloride at 20℃; for 0.5h; Acidic aq. solution; Inert atmosphere;A 15%
B 30%
phenyliminodiacetic acid diethyl ester
55932-12-2

phenyliminodiacetic acid diethyl ester

2,2'-(phenylimino)bis[ethanol]
120-07-0

2,2'-(phenylimino)bis[ethanol]

Conditions
ConditionsYield
With lithium aluminium tetrahydride In tetrahydrofuran Ambient temperature;26%
With lithium aluminium tetrahydride In tetrahydrofuran at 80℃; for 2h;
2-Amino-6-bromopyridine
19798-81-3

2-Amino-6-bromopyridine

pyridine-2-boronic acid N-phenyldiethanolamine ester
882521-96-2

pyridine-2-boronic acid N-phenyldiethanolamine ester

A

6-amino-2-2’-pyridylbipyridine
178039-84-4

6-amino-2-2’-pyridylbipyridine

B

2,2'-(phenylimino)bis[ethanol]
120-07-0

2,2'-(phenylimino)bis[ethanol]

Conditions
ConditionsYield
With copper(l) iodide; tetrakis(triphenylphosphine) palladium(0); potassium carbonate In tetrahydrofuran for 24h; Suzuki-Miyaura cross-coupling; Reflux; Inert atmosphere;
6-bromopyridine-3-amine
13534-97-9

6-bromopyridine-3-amine

pyridine-2-boronic acid N-phenyldiethanolamine ester
882521-96-2

pyridine-2-boronic acid N-phenyldiethanolamine ester

A

2,2'-(phenylimino)bis[ethanol]
120-07-0

2,2'-(phenylimino)bis[ethanol]

B

[2,2’-bipyridin]-5-amine
160539-04-8

[2,2’-bipyridin]-5-amine

Conditions
ConditionsYield
With copper(l) iodide; tetrakis(triphenylphosphine) palladium(0); potassium carbonate In tetrahydrofuran for 24h; Suzuki-Miyaura cross-coupling; Reflux; Inert atmosphere;
[1,3]-dioxolan-2-one
96-49-1

[1,3]-dioxolan-2-one

2-Anilinoethanol
122-98-5

2-Anilinoethanol

A

carbon dioxide
124-38-9

carbon dioxide

B

2,2'-(phenylimino)bis[ethanol]
120-07-0

2,2'-(phenylimino)bis[ethanol]

Conditions
ConditionsYield
at 140℃; Kinetics; Neat (no solvent); chemospecific reaction;
methanol
67-56-1

methanol

acetone
67-64-1

acetone

N-methylaniline
100-61-8

N-methylaniline

A

2,2'-(phenylimino)bis[ethanol]
120-07-0

2,2'-(phenylimino)bis[ethanol]

B

C11H17NO
1413925-42-4

C11H17NO

C

N-(2-hydroxyethyl)-N-methylaminobenzene
93-90-3

N-(2-hydroxyethyl)-N-methylaminobenzene

D

2-Anilinoethanol
122-98-5

2-Anilinoethanol

Conditions
ConditionsYield
With tert.-butylhydroperoxide; titanium tetrachloride; zinc In water at 20℃; Inert atmosphere;A n/a
B 20 %Spectr.
C n/a
D n/a
2,2'-(phenylimino)bis[ethanol]
120-07-0

2,2'-(phenylimino)bis[ethanol]

tert-butyldimethylsilyl chloride
18162-48-6

tert-butyldimethylsilyl chloride

N,N-bis[2-[(1-tert-butyl-1,1-diemthylsilyl)oxy]ethyl]-N-phenylamine
148717-08-2

N,N-bis[2-[(1-tert-butyl-1,1-diemthylsilyl)oxy]ethyl]-N-phenylamine

Conditions
ConditionsYield
With 1H-imidazole In dichloromethane for 5h;100%
2,2'-(phenylimino)bis[ethanol]
120-07-0

2,2'-(phenylimino)bis[ethanol]

propargyl bromide
106-96-7

propargyl bromide

N,N-bis(2-(prop-2-ynyloxy)ethyl)aniline
1202493-52-4

N,N-bis(2-(prop-2-ynyloxy)ethyl)aniline

Conditions
ConditionsYield
With tetra(n-butyl)ammonium hydrogensulfate; sodium hydroxide In water; toluene at 20℃; for 24h;100%
With tetrabutylammomium bromide; sodium hydroxide In water; toluene at 20℃; for 3h;96%
With sodium hydride In N,N-dimethyl-formamide; toluene; mineral oil at 0 - 20℃; for 1h; Inert atmosphere;72%
With tetrabutylammomium bromide; potassium hydroxide In dimethyl sulfoxide at 60℃; for 24h;55%
With potassium hydroxide In dimethyl sulfoxide at 50℃; for 120h;
2,2'-(phenylimino)bis[ethanol]
120-07-0

2,2'-(phenylimino)bis[ethanol]

methanesulfonyl chloride
124-63-0

methanesulfonyl chloride

N,N-bis<2-<(methylsulfonyl)oxy>ethyl>aniline
22964-38-1

N,N-bis<2-<(methylsulfonyl)oxy>ethyl>aniline

Conditions
ConditionsYield
With triethylamine In chloroform at 0℃; for 1h;99.6%
With triethylamine In dichloromethane at 20℃; for 1h;96.4%
With triethylamine In ethyl acetate at 20℃; for 1h;89%
2,2'-(phenylimino)bis[ethanol]
120-07-0

2,2'-(phenylimino)bis[ethanol]

1-bromo-4-benzene
13165-33-8

1-bromo-4-benzene

Conditions
ConditionsYield
With methanol; tetraethylammonium chloride; bromine In dichloromethane at 35℃;99%
With periodic acid; sodium bromide In water at 20℃; for 0.166667h; regioselective reaction;93%
With N-Bromosuccinimide In dichloromethane at 20℃; for 24h; Darkness;89%
2,2'-(phenylimino)bis[ethanol]
120-07-0

2,2'-(phenylimino)bis[ethanol]

t-butyldimethylsiyl triflate
69739-34-0

t-butyldimethylsiyl triflate

N,N-bis[2-[(1-tert-butyl-1,1-diemthylsilyl)oxy]ethyl]-N-phenylamine
148717-08-2

N,N-bis[2-[(1-tert-butyl-1,1-diemthylsilyl)oxy]ethyl]-N-phenylamine

Conditions
ConditionsYield
With 2,6-dimethylpyridine In dichloromethane at -80 - 20℃; for 1h; silylation;99%
2,2'-(phenylimino)bis[ethanol]
120-07-0

2,2'-(phenylimino)bis[ethanol]

acetyl chloride
75-36-5

acetyl chloride

bis(2-acetoxyethyl)aniline
19249-34-4

bis(2-acetoxyethyl)aniline

Conditions
ConditionsYield
With triethylamine In tetrahydrofuran at 35℃; for 15h;99%
With triethylamine In tetrahydrofuran98%
With triethylamine In dichloromethane at 20 - 25℃; for 2h; Cooling with ice;96%
2,2'-(phenylimino)bis[ethanol]
120-07-0

2,2'-(phenylimino)bis[ethanol]

5-phenyl-(2,8-dioxa-5-aza-1-stanna)bicyclo[3.3.01.5]octane

5-phenyl-(2,8-dioxa-5-aza-1-stanna)bicyclo[3.3.01.5]octane

Conditions
ConditionsYield
In toluene Inert atmosphere; Schlenk technique;99%
4-iodobenzoic acid
619-58-9

4-iodobenzoic acid

2,2'-(phenylimino)bis[ethanol]
120-07-0

2,2'-(phenylimino)bis[ethanol]

C24H21I2NO4
1436920-32-9

C24H21I2NO4

Conditions
ConditionsYield
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 0℃; for 3h;98.8%
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 20℃; for 72h;98.8%
4-iodobenzoic acid
619-58-9

4-iodobenzoic acid

2,2'-(phenylimino)bis[ethanol]
120-07-0

2,2'-(phenylimino)bis[ethanol]

C25H23I2NO3

C25H23I2NO3

Conditions
ConditionsYield
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 20℃; for 72h;98.8%
2,2'-(phenylimino)bis[ethanol]
120-07-0

2,2'-(phenylimino)bis[ethanol]

5-amino-3-methyl-thiophene-2,4-dicarbonitrile
52603-48-2

5-amino-3-methyl-thiophene-2,4-dicarbonitrile

C17H17N5O2S
162245-60-5

C17H17N5O2S

Conditions
ConditionsYield
Stage #1: 5-amino-3-methyl-thiophene-2,4-dicarbonitrile With nitrosylsulfuric acid; sulfuric acid; acetic acid; propionic acid at 0 - 5℃; for 1h;
Stage #2: 2,2'-(phenylimino)bis[ethanol] With acetic acid In water Cooling with ice;
Stage #3: With ammonia In water pH=4;
98%
2,2'-(phenylimino)bis[ethanol]
120-07-0

2,2'-(phenylimino)bis[ethanol]

benzoyl chloride
98-88-4

benzoyl chloride

2-[phenyl(2-benzoyloxyethyl)amino]ethyl benzoate
24867-51-4

2-[phenyl(2-benzoyloxyethyl)amino]ethyl benzoate

Conditions
ConditionsYield
With triethylamine In dichloromethane at 20℃; for 24h; Acylation;97%
With triethylamine In dichloromethane at 0℃; for 3h; Acylation;86%
2,2'-(phenylimino)bis[ethanol]
120-07-0

2,2'-(phenylimino)bis[ethanol]

N,N-dimethyl-formamide
68-12-2, 33513-42-7

N,N-dimethyl-formamide

4-(bis(2-chloroethyl)amino)benzaldehyde
1208-03-3

4-(bis(2-chloroethyl)amino)benzaldehyde

Conditions
ConditionsYield
Stage #1: 2,2'-(phenylimino)bis[ethanol]; N,N-dimethyl-formamide With trichlorophosphate at 0 - 40℃; for 8h; Vilsmeier-Haack formylation; Inert atmosphere;
Stage #2: With potassium carbonate In water Cooling with ice;
97%
Stage #1: N,N-dimethyl-formamide With trichlorophosphate In water; N,N-dimethyl-formamide at 0℃; for 0.75h;
Stage #2: 2,2'-(phenylimino)bis[ethanol] In water; N,N-dimethyl-formamide at 0 - 110℃; for 2h;
96%
With trichlorophosphate at 90℃; for 2h;95%

120-07-0Relevant articles and documents

A BODIPY-based fluorescent sensor for the detection of Pt2+ and Pt drugs

Bian, Qingyuan,Kong, Fred Ka-Wai,Leung, Ken Cham-Fai,Ng, Maggie,Tang, Fung-Kit,Tse, Anfernee Kai-Wing,Tse, Yu-Chung,Yam, Vivian Wing-Wah,Zhu, Jiaqian

, p. 2695 - 2698 (2020)

A BODIPY-based fluorescent sensor PS with an NO4S2 podand ligand was studied for the selective detection of Pt2+ over 21 cations as well as selected platinum drugs in aqueous medium. The platinum sensor PS shows 28-fold, 22-fold and 14-fold fluorescence turn-on enhancements to Pt2+, cisplatin and nedaplatin, and was thereby employed to detect platinum drugs in A-549 human lung cancer cells.

Kinetic parameter estimation of solvent-free reactions monitored by 13C NMR spectroscopy, a case study: Mono- and di-(hydroxy)ethylation of aniline with ethylene carbonate

Lucchini, Vittorio,Fabris, Massimo,NoE, Marco,Perosa, Alvise,Selva, Maurizio

, p. 154 - 160 (2011)

The kinetics of solvent-free reactions can be followed in situ by 13C nuclear magnetic resonance (NMR) spectroscopy, provided that the reaction mixture can be maintained liquid at the monitoring temperature. The pros and cons of the technique and the correct translation of the signal intensities into concentrations are discussed. A good model for this investigation is the reaction of ethylene carbonate (1) with aniline (2) at 140°C, two alkylation products of N-mono- and N, N-bis-(2-hydroxy)ethylation of aniline form (compounds 3 and 4, respectively). The overall reaction occurs with heavy volume shrinking, so that the physical as well as the chemical features evolve during the course of the process. The chemical evolution is described by the kinetic constants k1 and k2 of the two N-alkylation steps, the physical evolution by the time-dependent activity coefficients α(t). Two complementary procedures are utilized for the determination of these parameters.

Synthesis of New Bis-1,2,4-Oxadiazoline Derivatives via 1,3-Dipolar Cycloaddition Reaction

Chen, Fei,Zeng, Hua,Liu, Fang-Ming

, p. 1866 - 1870 (2016)

A series of novel bis-oxadiazoline derivatives 4 was synthesized via 1,3-dipolar cycloaddition reaction of bis-aldimines 3, and nitrile oxides generated in situ from various benzohydroximinoyl chlorides in the presence of Et3N. The target products were confirmed by IR,1H-NMR, and mass spectrometry.

-

Adkins,Simington

, p. 1687,1688 (1925)

-

Synthesis, characterization and properties of NLO dye-containing polyurethane

Moon,Shim,Lee

, p. 91 - 97 (1994)

Polyurethane attached hemicyanine dye with tetraphenylborate anion was synthesized. This polymer was soluble in dimethylformamide and could be processed into thin film by spin coating. The poled polymer film showed a large second-order nonlinear optical coefficient (χ(2) = 4.0×10-7 esu) and good temporal stability.

A water-soluble BODIPY based ‘OFF/ON' fluorescent probe for the detection of Cd2+ ions with high selectivity and sensitivity

Maity, Apurba,Ghosh, Utsav,Giri, Dipanjan,Mukherjee, Devdeep,Maiti, Tapas Kumar,Patra, Sanjib K.

supporting information, p. 2108 - 2117 (2019/02/12)

A water-soluble dilithium salt BODIPY derivative (LiBDP) with appended dicarboxylate pseudo-crown ether [NO4] coordinating sites has been designed, synthesized and characterized successfully for the selective and sensitive recognition of Cd2+ in aqueous media. The chemosensor exhibits a remarkable increase in fluorescence intensity as well as a distinct color change upon the addition of Cd2+ over other environmentally and biologically relevant metal ions in H2O. The fluorometric response of LiBDP is attributed to the metal chelation-enhanced fluorescence (MCHEF) effect which has been confirmed by a strong association constant of 2.57 ± 1.06 × 105 M?1 and Job's plot, indicating 1?:?1 binding stoichiometry between LiBDP and Cd2+. Frontier molecular orbital analysis (obtained from DFT studies) also illustrates the turn-on fluorescence of the probe by blocking photoinduced electron transfer (PET) after coordination to Cd2+. The probe can detect Cd2+ in a competitive environment up to a submicromolar level in a biologically significant pH range. The sensor is proved to be reversible and reusable by the alternative addition of Cd2+ followed by S2?. The OFF/ON/OFF sensing behavior is utilized to construct an INHIBIT molecular logic gate based on the two inputs of Cd2+ and S2? and a fluorescence intensity at 512 nm as an output. The test paper experiment demonstrates the practical utility of LiBDP to monitor Cd2+ in an aqueous sample. Finally, the sensing probe was utilized to monitor Cd2+ in living cells.

A straightforward one-pot synthesis of bioactive: N -aryl oxazolidin-2-ones via a highly efficient Fe3O4@SiO2-supported acetate-based butylimidazolium ionic liquid nanocatalyst under metal- and solvent-free conditions

Gupta, Radhika,Yadav, Manavi,Gaur, Rashmi,Arora, Gunjan,Sharma, Rakesh Kumar

, p. 3801 - 3812 (2017/08/22)

In the present study, we report the fabrication and characterization of novel acetate-based butylimidazolium ionic liquid immobilized silica-coated magnetic nanoparticles (IL-OAc@FSMNP). The synthesized nanocomposite proves its supremacy as an environmentally benign catalyst in the reaction of aniline and its derivatives with ethylene carbonate to form bioactive N-aryl oxazolidin-2-ones under metal-, ligand-, and solvent-free conditions. The catalyst offers excellent assemblies of hydrogen-bond donors and acceptors, which activate the substrates, thereby delivering good-to-excellent product yields with a conversion and selectivity of more than 99%. Additionally, mild reaction conditions, wide substrate scope, effortless catalytic recovery and recyclability of the catalyst up to eight consecutive cycles offer the potential for scale-up in various pharmaceutical applications.

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