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"5-[3,4-bis(benzyloxy)benzylidene]imidazolidine-2,4-dione" is a complex organic compound with the molecular formula C26H22N2O4. It features a central imidazolidine-2,4-dione ring, which is a five-membered ring containing two nitrogen atoms and two carbonyl groups. The compound is characterized by a benzylidene group attached to the 5-position of the imidazolidine ring, with the benzene ring of the benzylidene group having two benzyloxy substituents at the 3 and 4 positions. These benzyloxy groups are protective groups for the hydroxyl groups, which can be removed under certain conditions to reveal the free hydroxyl groups. 5-[3,4-bis(benzyloxy)benzylidene]imidazolidine-2,4-dione is often used in organic synthesis, particularly in the preparation of pharmaceuticals and other complex molecules, due to its ability to undergo further chemical reactions and transformations.

4816-03-9

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4816-03-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4816-03-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,1 and 6 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4816-03:
(6*4)+(5*8)+(4*1)+(3*6)+(2*0)+(1*3)=89
89 % 10 = 9
So 4816-03-9 is a valid CAS Registry Number.

4816-03-9SDS

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 5-(3,4,5-trimethoxy-phenyl)-valeric acid

1.2 Other means of identification

Product number -
Other names 5-(3,4,5-Trimethoxy-phenyl)-valeriansaeure

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

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More Details:4816-03-9 SDS

4816-03-9Relevant academic research and scientific papers

Synthesis and spectroscopic characterization of model compounds for the active site cofactor in copper amine oxidases

Mure, Minae,Klinman, Judith P.

, p. 7117 - 7127 (2007/10/02)

The synthesis and spectroscopic characterization of compounds which model different forms of the active site cofactor in copper amine oxidases have been pursued. As described, 5-(2,4,5-trihydroxybenzyl)hydantoin (1redH3), its corresp

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