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2-Azetidinone, 3-(1-hydroxyethyl)-1-(phenylmethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

80756-83-8

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80756-83-8 Usage

Main Properties

Belongs to the azetidinone class of compounds
Cyclic β-lactam ring structure
Substituent attached to the nitrogen atom
Contains a 1-hydroxyethyl group and a phenylmethyl group

Specific Content

Chemical compound with a unique structure
Potential applications in the pharmaceutical industry
Versatile intermediate for the synthesis of pharmaceuticals and organic compounds
May have significant pharmacological properties and bioactivities.

Check Digit Verification of cas no

The CAS Registry Mumber 80756-83-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,7,5 and 6 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 80756-83:
(7*8)+(6*0)+(5*7)+(4*5)+(3*6)+(2*8)+(1*3)=148
148 % 10 = 8
So 80756-83-8 is a valid CAS Registry Number.

80756-83-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-benzyl-3-(1-hydroxyethyl)azetidin-2-one

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:80756-83-8 SDS

80756-83-8Downstream Products

80756-83-8Relevant academic research and scientific papers

STANNOUS TRIFLATE MEDIATED ALDOL REACTION OF 3-(3-ALKOXY AND 3-AMINOPROPANOYL)THIAZOLIDINE-2-THIONES STEREOSELECTIVE SYNTHESIS OF β-LACTAM DERIVATIVES

Iwasawa, Nobuharu,Huang, Huamin,Mukaiyama, Teruaki

, p. 1045 - 1048 (2007/10/02)

The tin(II) enolate is generated from 3-acylthiazolidine-2-thione with β-alkoxy or β-amino functionality on treatment with stannous triflate in the presence of N-ethylpiperidine.The enolate further reacts with aldehyde to afford the aldol product with high syn-stereoselectivity.The aldol product thus produced is stereospecifically converted to β-lactam derivative with hydroxyethyl side chain.

Synthesis of β-Lactams from ?-Allyltricarbonyliron (Lactone) Complexes

Annis, Gary D.,Hebblethwaite, Elizabeth M.,Hodgson, Simon T.,Hollinshead, David M.,Ley, Steven V.

, p. 2851 - 2856 (2007/10/02)

Several ?-allyltricarbonyliron (lactone) complexes have been treated with an excess of benzylamine in the presence of Lewis acids to afford the corresponding lactam complexes by SN2'-like process.These lactam complexes were oxidised in good yie

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