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41730-79-4

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    Cas No: 41730-79-4

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41730-79-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 41730-79-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,7,3 and 0 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 41730-79:
(7*4)+(6*1)+(5*7)+(4*3)+(3*0)+(2*7)+(1*9)=104
104 % 10 = 4
So 41730-79-4 is a valid CAS Registry Number.
InChI:InChI=1/C4H8N2O3S/c1-10(8,9)6-3-2-5-4(6)7/h2-3H2,1H3,(H,5,7)

41730-79-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Methanesulfonyl-2-imidazolidinone

1.2 Other means of identification

Product number -
Other names 1-methylsulfonylimidazolidin-2-one

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:41730-79-4 SDS

41730-79-4Relevant articles and documents

Synthesis of oxazolidin-2-ones and imidazolidin-2-ones directly from 1,3-diols or 3-amino alcohols using iodobenzene dichloride and sodium azide

He, Tian,Gao, Wen-Chao,Wang, Wei-Kun,Zhang, Chi

, p. 1113 - 1118 (2014/04/03)

A general and efficient method for the synthesis of oxazolidin-2-ones and imidazolidin-2-ones directly from 1,3-diols and 3-amino alcohols has been developed using the same reagent combination of iodobenzene dichloride (PhICl2) and sodium azide (NaN3).

Mezlocillin: A Penicillin from the Acylureido Series / Synthesis and chemical properties

Koenig, H.-B.,Metzger, K. G.,Offe, H.-A.,Schroeck, W.

, p. 88 - 90 (2007/10/02)

Mezlocillin, 6--penicillanic acid, is a new semisynthetic acylureido-penicillin with a broad spectrum of antibacterial activity.The synthesis of mezlocillin from ampicillin and the from 6-aminopenicillanic acid and the physico-chemical properties are described.Mezlocillin is cleaved by penicillinase to the penicilloate which is degraded further by acids to the penilloate. - Key words: Acylureido series; Mezlocillin, chemical properties, synthesis; Penicillins

Penicillins

-

, (2008/06/13)

Arylmethyl- and cyclohexenylmethyl- penicillins, substituted on the α-carbon atom of the side chain by a 2,3-disubstituted imidazolidinylcarbamido or a 2,3-disubstituted imidazolidinylthiocarbamido group, or by the corresponding 2,3-disubstituted 1,3-diazacyclohexylcarbamido or thiocarbamido groups are anti-bacterial agents.

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