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2,2'-(BENZYLIMINO)DIETHANOL

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Products Intro: Product Name:2-[benzyl(2-hydroxyethyl)amino]ethan-1-ol
CAS:101-32-6
Purity:0.99 Package:2.5KG;500G
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Products Intro: Product Name:2-[2-Hydroxyethyl(phenylmethyl)amino]ethanol
CAS:101-32-6
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Products Intro: Product Name:2,2'-(BENZYLIMINO)DIETHANOL
CAS:101-32-6
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Products Intro: Product Name:2,2'-(BENZYLIMINO)DIETHANOL
CAS:101-32-6
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Products Intro: Product Name:2-[benzyl(2-hydroxyethyl)amino]ethan-1-ol
CAS:101-32-6

2,2'-(BENZYLIMINO)DIETHANOL manufacturers

2,2'-(BENZYLIMINO)DIETHANOL Basic information
Uses
Product Name:2,2'-(BENZYLIMINO)DIETHANOL
Synonyms:BUTTPARK 145\50-27;2-[BENZYL(2-HYDROXYETHYL)AMINO]-1-ETHANOL;N-BENZYLDIETHANOLAMINE;N,N-BIS(HYDROXYETHYL)-BENZYLAMINE;2,2’-((phenylmethyl)imino)bis-ethano;2,2’-(benzylimino)di-ethano;benzylbis(2-hydroxyethyl)amine;benzyldiethanolamine
CAS:101-32-6
MF:C11H17NO2
MW:195.26
EINECS:202-934-6
Product Categories:
Mol File:101-32-6.mol
2,2'-(BENZYLIMINO)DIETHANOL Structure
2,2'-(BENZYLIMINO)DIETHANOL Chemical Properties
Melting point 196.5 °C(Solv: benzene (71-43-2))
Boiling point 226°C(lit.)
density 1.09
refractive index 1.5370 to 1.5410
storage temp. Inert atmosphere,Room Temperature
pka14.39±0.10(Predicted)
form clear liquid
color Colorless to Yellow to Orange
InChIInChI=1S/C11H17NO2/c13-8-6-12(7-9-14)10-11-4-2-1-3-5-11/h1-5,13-14H,6-10H2
InChIKeyMIZIOHLLYXVEHJ-UHFFFAOYSA-N
SMILESN(CCO)(CCO)CC1=CC=CC=C1
CAS DataBase Reference101-32-6(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
RTECS KJ7538000
HazardClass IRRITANT
HS Code 2922190090
MSDS Information
2,2'-(BENZYLIMINO)DIETHANOL Usage And Synthesis
Uses2,2'-(Benzylazanediyl)diethanol is a useful research chemical.
Synthesis
Benzyl bromide

100-39-0

Diethanolamine

111-42-2

2,2'-(BENZYLIMINO)DIETHANOL

101-32-6

General procedure for the synthesis of 2,2-(benzylimino)diethanol from benzyl bromide and diethanolamine: K2CO3 (8.65 g, 62.58 mmol) and benzyl bromide (2.96 g, 25 mmol) were added to anhydrous acetone (65 mL) followed by diethanolamine (2.63 g, 53.08 mmol). The reaction mixture was heated to reflux and the reaction was continued overnight. After completion of the reaction, the white suspension obtained was filtered and the solvent was removed by evaporation to obtain 5.6 g of yellow liquid. The liquid was dissolved in dichloromethane (DCM) and washed with deionized water. The organic layer was dried over anhydrous sodium sulfate and concentrated in vacuum to give the final 2,2-(benzylimino)diethanol (4.88 g, 100% yield). The product was analyzed by HPLC-MS (Method A): retention time 1.14 min; ESI-MS m/z 196 ([M+H]+).

References[1] Inorganic Chemistry, 2012, vol. 51, # 19, p. 10384 - 10393,10
[2] Patent: WO2017/16669, 2017, A1. Location in patent: Page/Page column 201
[3] Journal of Medicinal Chemistry, 2003, vol. 46, # 12, p. 2376 - 2396
[4] Patent: EP970046, 2003, B1. Location in patent: Page 45-46
[5] Patent: US6342508, 2002, B1. Location in patent: Page column 58-59
Tag:2,2'-(BENZYLIMINO)DIETHANOL(101-32-6) Related Product Information
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