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2H-Imidazol-2-one, 4-(3-amino-1-methoxypropyl)-1,3-dihydro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

308103-74-4

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308103-74-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 308103-74-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,8,1,0 and 3 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 308103-74:
(8*3)+(7*0)+(6*8)+(5*1)+(4*0)+(3*3)+(2*7)+(1*4)=104
104 % 10 = 4
So 308103-74-4 is a valid CAS Registry Number.

308103-74-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(3-amino-1-methoxypropyl)-1,3-dihydro-2-imidazolone

1.2 Other means of identification

Product number -
Other names 4-(3-Amino-1-methoxy-propyl)-1,3-dihydro-imidazol-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:308103-74-4 SDS

308103-74-4Downstream Products

308103-74-4Relevant academic research and scientific papers

Synthesis of axinohydantoins

Barrios Sosa, Ana Carolina,Yakushijin, Kenichi,Horne, David A.

, p. 4498 - 4500 (2002)

A short synthesis of the hydantoin-containing marine sponge metabolites axinohydantoins is described. A key feature of the synthesis is a putative biomimetic, intramolecular cyclization of α-functionalized imidazolone 5, which affords the tricyclic pyrroloazepinone framework comprising 6. In addition, the conversion of imidazolones to α,β-unsaturated hydantoins is outlined and represents a new approach to these heterocyclic systems.

Synthesis of slagenins A, B, and C.

Barrios Sosa,Yakushijin,Horne

, p. 3443 - 3444 (2000)

[structure: see text] A short synthesis of the marine sponge metabolites slagenins A (1), B (2), and C (3) is described. The synthetic route features the preparation of beta-hydroxyimidazolone 4 from ornithine and its subsequent oxidative cyclization to the slagenin core.

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