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N-(p-Nitrobenzoyl)glutaMic Acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

22536-03-4

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22536-03-4 Usage

Uses

N-(p-Nitrobenzoyl)glutamic Acid is a derivative of L-Glutamic Acid (G596960), a non-essential amino acid. Its salt form (glutamate) is an important neurotransmitter that plays a key role in long-term potentiation and is important for learning and memory.

Check Digit Verification of cas no

The CAS Registry Mumber 22536-03-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,5,3 and 6 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 22536-03:
(7*2)+(6*2)+(5*5)+(4*3)+(3*6)+(2*0)+(1*3)=84
84 % 10 = 4
So 22536-03-4 is a valid CAS Registry Number.

22536-03-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name p-NO2C6H4CONHCH(CH2CH2COOH)COOH

1.2 Other means of identification

Product number -
Other names L-N-p-nitrobenzoylglutamic acid

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:22536-03-4 SDS

22536-03-4Relevant academic research and scientific papers

Synthesis, characterization and biological activity of Cu(II) chelates with some amino acid derivatives

Nandi, M. M.,Choudhury, J.,Tarat, S.

, p. 288 - 291 (2007/10/02)

The complexing behaviour of seventeen amino acid derivatives towards Cu(II) has been studied.Complexes of the types Cu(RH)*xH2O, Cu(RH).Cu(OH)2*xH2O and Cu(R'H)2*yH2O have been prepared and characterized by IR, ESR, electronic spectral, magnetic moment and analytical data.On the basis of differences and direction of the shifts in the IR frequencies of vas OCO and vs OCO modes and ESR spectra, bonding modes of carboxylate group have been established.Biological activitu of complexes is more than that of the free metal ion and the ligands.

New glutamic and aspartic derivatives with potent CCK-antagonistic activity

Makovec,Chiste,Bani,et al.

, p. 9 - 20 (2007/10/02)

New derivatives of aspartic and glutamic acid were synthesized and evaluated in vitro and in vivo for anti-CCK activity on the guinea pig gallbladder. The anti-CCK activity of some 4-benzamido-glutaramic acid derivatives was a hundred times greater than that of proglutamide, the model compound, and they have been selected for further studies.

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