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Carbamic acid, (3-methoxy-2-oxo-3-azetidinyl)-, phenylmethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

78184-08-4

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78184-08-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 78184-08-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,1,8 and 4 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 78184-08:
(7*7)+(6*8)+(5*1)+(4*8)+(3*4)+(2*0)+(1*8)=154
154 % 10 = 4
So 78184-08-4 is a valid CAS Registry Number.

78184-08-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name benzyl N-(3-methoxy-2-oxoazetidin-3-yl)carbamate

1.2 Other means of identification

Product number -
Other names benzyl 3-methoxy-2-oxo-3-azetidinylcarbamate

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:78184-08-4 SDS

78184-08-4Relevant academic research and scientific papers

2-OXO-1-AZETIDINESULFONIC ACID SALTS

-

, (2008/06/13)

Antibacterial activity is exhibited by beta-lactams having a sulfonic acid salt substituent in the 1-position and an amino or acylamino substituent in the 3-position.

Synthesis and antibacterial activity of 3-acylamino-3-methoxy-2-azetidinone-1-sulfonic acid derivatives

Matsuo,Masuya,Sugawara,Kawano,Noguchi,Ochiai

, p. 2200 - 2208 (2007/10/02)

As a key intermediate for the synthesis of sulfazecin derivatives, 3-amino-3-methoxy-2-azetidinone (24 or 26) was synthesized from penicillins, and various new compounds, including sulfazecin, were synthesized by acylation and sulfonation of 24 or 26. Som

Monobactams. The Conversion of 6-APA to (S)-3-Amino-2-oxoazetidine-1-sulfonic Acid and Its 3(RS)-Methoxy Derivative

Cimarusti, C. M.,Applegate, H. E.,Chang, H. W.,Floyd, D. M.,Koster, W. H.,et al.

, p. 179 - 180 (2007/10/02)

A facile conversion of 6-APA to (S)-3-aminomonobactamic acid (3-AMA) and its 3(RS)-methoxy derivative, key intermediates for the synthesis of 3-(acylamino)-2-oxoazetidine-1-sulfonic acids (monobactams), is described.

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