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2,5-Pyrrolidinedione, 1-[(4-azido-2-hydroxy-5-iodobenzoyl)oxy]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

99298-06-3

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99298-06-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 99298-06-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,2,9 and 8 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 99298-06:
(7*9)+(6*9)+(5*2)+(4*9)+(3*8)+(2*0)+(1*6)=193
193 % 10 = 3
So 99298-06-3 is a valid CAS Registry Number.

99298-06-3SDS

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 (2,5-dioxopyrrolidin-1-yl) 4-azido-2-hydroxy-5-iodobenzoate

1.2 Other means of identification

Product number -
Other names 2,5-Pyrrolidinedione,1-[(4-azido-2-hydroxy-5-iodobenzoyl)oxy]

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:99298-06-3 SDS

99298-06-3Relevant articles and documents

Design and synthesis of photoaffinity-labeling ligands of the L-prolyl-L-leucylglycinamide binding site involved in the allosteric modulation of the dopamine receptor

Fisher, Abigail,Mann, Amandeep,Verma, Vaneeta,Thomas, Nancy,Mishra, Ram K.,Johnson, Rodney L.

, p. 307 - 317 (2007/10/03)

Pro-Leu-Gly-NH2 (PLG), in addition to its endocrine effects, possesses the ability to modulate dopamine 02 receptors within the central nervous system. However, the precise binding site of PLG is unknown. Potential photoaffinity-labeling ligand

Synthesis and biological activity of iodinated and photosensitive derivatives of tetrabenazine

Aranda,Beaucourt,Ponchant,Isambert,Henry

, p. 369 - 374 (2007/10/02)

The synthesis of a photosensitive iodinated derivative of tetrabenazine, which should be able to lead to the identification of the vesicular catecholamine transporter of adrenal medulla by photoaffinity, is described in detail. The biological activity of this iodinated ligand was found to be significantly lower than that of non iodinated ligands.

IODINATION OF PHENOLS USING CHLORAMINE T AND SODIUM IODIDE

Kometani, Tadashi,Watt, David S.,Ji, Tae

, p. 2043 - 2046 (2007/10/02)

A convenient procedure for the iodination of many substituted phenols uses chloramine T and sodium iodide in DMF, DMSO, or acetonitrile.

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