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Glycine, N,N'-[[[(4-methylphenyl)sulfonyl]imino]di-2,1-ethanediyl]bis[N-[(4-methylphenyl)sulfonyl]-, dimethyl ester is a complex organic compound that incorporates glycine, a non-essential amino acid, along with sulfonyl groups and ethanediyl chains. Glycine,
N,N'-[[[(4-methylphenyl)sulfonyl]imino]di-2,1-ethanediyl]bis[N-[(4-methyl
phenyl)sulfonyl]-, dimethyl ester is characterized by its dimethyl ester functional group, which is bonded to two methyl groups. The sulfonyl groups present in the molecule indicate potential applications in medicinal chemistry, as sulfonyl compounds are recognized for their wide range of biological activities. Further research and testing are required to explore the specific properties and uses of Glycine, N,N'-[[[(4-methylphenyl)sulfonyl]imino]di-2,1-ethanediyl]bis[N-[(4-methyl phenyl)sulfonyl]-, dimethyl ester.

110345-43-2

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110345-43-2 Usage

Uses

Used in Pharmaceutical Research:
Glycine, N,N'-[[[(4-methylphenyl)sulfonyl]imino]di-2,1-ethanediyl]bis[N-[(4-methylphenyl)sulfonyl]-, dimethyl ester is used as a research compound for its potential applications in the development of new pharmaceuticals. The presence of sulfonyl groups and the unique structure of the molecule make it a candidate for investigation in medicinal chemistry.
Used in Organic Synthesis:
In the field of organic synthesis, Glycine, N,N'-[[[(4-methylphenyl)sulfonyl]imino]di-2,1-ethanediyl]bis[N-[(4-methylphenyl)sulfonyl]-, dimethyl ester serves as a key intermediate or building block for the synthesis of more complex molecules. Its structural features, including the glycine backbone and sulfonyl groups, can be exploited to create novel compounds with potential applications in various industries.
Used in Chemical Research:
Glycine, N,N'-[[[(4-methylphenyl)sulfonyl]imino]di-2,1-ethanediyl]bis[N-[(4-methylphenyl)sulfonyl]-, dimethyl ester is used as a subject of study in chemical research to understand its reactivity, stability, and potential interactions with other molecules. This knowledge can contribute to the advancement of chemical science and the discovery of new applications for the compound.

Check Digit Verification of cas no

The CAS Registry Mumber 110345-43-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,3,4 and 5 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 110345-43:
(8*1)+(7*1)+(6*0)+(5*3)+(4*4)+(3*5)+(2*4)+(1*3)=72
72 % 10 = 2
So 110345-43-2 is a valid CAS Registry Number.

110345-43-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N',N''-Tris(p-tolylsulfonyl)-3,6,9-triazundecanedioic acid dimethyl ester

1.2 Other means of identification

Product number -
Other names [{2-[{2-[Methoxycarbonylmethyl-(toluene-4-sulfonyl)-amino]-ethyl}-(toluene-4-sulfonyl)-amino]-ethyl}-(toluene-4-sulfonyl)-amino]-acetic acid methyl ester

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:110345-43-2 SDS

110345-43-2Upstream product

110345-43-2Relevant academic research and scientific papers

Manganese complexes of nitrogen-containing macrocyclic ligands effective as catalysts for dismutating superoxide

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, (2008/06/13)

The present invention is directed to low molecular weight mimics of superoxide dismutase (SOD) represented by the formula: STR1 wherein R, R', R1, R'1, R2, R'2, R3, R'3, R4, R'4, R5, R'5, R6, R'6, R7, R'7, R8, R'8, R9, and R'9 and X, Y, Z and n are as defined herein, useful as therapeutic agents for inflammatory disease states and disorders, ischemic/reperfusion injury, stroke, atherosclerosis, hypertension and all other conditions of oxidant-induced tissue damage or injury.

Methods of preparing manganese complexes of nitrogen-containing macrocyclic ligands

-

, (2008/06/13)

The present invention is directed to low molecular weight mimics of superoxide dismutase (SOD) represented by the formula: STR1 wherein R, R', R1, R'1, R2, R'2, R3, R'3, R4, R'4, R5, R'5, R6, R'6, R7, R'7, R8, R'8, R9, and R'9 and X, Y, Z and n are as defined herein, useful as therapeutic agents for inflammatory disease states and disorders, ischemic/reperfusion injury, stroke, atherosclerosis, hypertension and all other conditions of oxidant-induced tissue damage or injury.

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