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Benzeneethanol, β-(diethylamino)-, also known as 2-(diethylamino)ethanolbenzene or phenethyl-β-(diethylamino)ethanol, is an organic compound with the chemical formula C12H19NO. It is a colorless to pale yellow liquid with a molecular weight of 191.29 g/mol. Benzeneethanol, b-(diethylamino)- is characterized by the presence of a benzene ring attached to an ethanol group, with a diethylamino group (-N(C2H5)2) at the β-position relative to the hydroxyl group. It is used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. Due to its amine group, it can undergo various chemical reactions, such as acylation, alkylation, and condensation, making it a versatile building block in organic synthesis.

7550-22-3

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7550-22-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7550-22-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,5 and 0 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 7550-22:
(6*7)+(5*5)+(4*5)+(3*0)+(2*2)+(1*2)=93
93 % 10 = 3
So 7550-22-3 is a valid CAS Registry Number.

7550-22-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(diethylamino)-2-phenylethan-1-ol

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
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:7550-22-3 SDS

7550-22-3Downstream Products

7550-22-3Relevant academic research and scientific papers

Synthesis of nanoporous aluminosilicate materials and their application as highly selective heterogeneous catalysts for the synthesis of β-amino alcohols

Robinson, Mathew W.C.,Davies, A. Matthew,Mabbett, Ian,Davies, Thomas E.,Apperley, David C.,Taylor, Stuart H.,Graham, Andrew E.

scheme or table, p. 57 - 63 (2010/11/04)

The ability of nanoporous aluminosilicate materials, synthesized using an evaporation-induced self-assembly (EISA) approach, to function as catalysts for the formation of β-amino alcohols from aromatic amines and epoxides was assessed. Materials containing high aluminium loadings displayed catalytic activity, giving the desired β-amino alcohols in high yield and with high selectivity for the Markovnikov addition product. These materials exhibited nanoporous pores, typically 1.34-1.49 nm, with a narrow pore size distribution and the expected large surface areas.

Transition metal-based lewis acid catalyzed ring opening of epoxides using amines under solvent-free conditions

Zhao, Pei-Qing,Xu, Li-Wen,Xia, Chun-Gu

, p. 846 - 850 (2007/10/03)

Transition metal-based Lewis acids, such as SnCl4·5H 2O, Co(OAc)2·4H2O, Ni(OAc) 2·2H2O, NiCl2, Mn(OAc) 2·4H2O etc. catalyze the nucleophilic opening of epox

AMINOLEAD COMPOUNDS AS A NEW REAGENT FOR REGIOSELECTIVE RING OPENING OF EPOXIDES

Yamada, Jun-ichi,Yumoto, Masatoshi,Yamamoto, Yoshinori

, p. 4255 - 4258 (2007/10/02)

Regioselective ring opening of epoxides is accomplished by using aminolead compounds; the reagents attack the less hindered carbon of epoxide ring, and the amino alcohols are obtained in good yields.

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