What is the 3-anilinopropane-1,2-diol?

3-anilinopropane-1,2-diol is , while it's Molecular Formula is C9H13 N O2. Used in Pharmaceutical Industry: 3-anilinopropane-1,2-diol is used as an active pharmaceutical ingredient for its potential therapeutic effects. The presence of the anilino group may provide specific interactions with biological targets, making it a candidate for the development of new drugs. Used in Chemical Synthesis: In the chemical industry, 3-anilinopropane-1,2-diol can be used as a building block or intermediate in the synthesis of more complex organic compounds. The anilino group can be further modified or used as a starting point for the creation of various chemical products. Used in Material Science: 3-anilinopropane-1,2-diol may find applications in the development of new materials due to its unique chemical structure. The anilino group could potentially be utilized to create novel polymers or other materials with specific properties, such as improved conductivity or enhanced mechanical strength. Used in Research and Development: As a glycol derivative with a unique structure, 3-anilinopropane-1,2-diol can be employed in research and development for studying its properties and potential applications. This may include investigating its interactions with biological systems, its use in drug discovery, or its role in the synthesis of new compounds.

What is the CAS number for 3-anilinopropane-1,2-diol?

The CAS number of 3-anilinopropane-1,2-diol is 5840-15-3.

What is 3-anilinopropane-1,2-diol (5840-15-3) used for?

3-anilinopropane-1,2-diol, also known as ChEBI, is a glycol derivative of glycerol where one of the hydroxy groups is substituted by an anilino group. 3-anilinopropane-1,2-diol exhibits unique chemical properties due to the presence of the anilino group, which can potentially lead to various applications in different industries.InChI:InChI=1/C9H13NO2/c11-7-9(12)6-10-8-4-2-1-3-5-8/h1-5,9-12H,6-7H2

What is the 3-anilinopropane-1,2-diol?

3-anilinopropane-1,2-diol is , while it's Molecular Formula is C9H13 N O2. Used in Pharmaceutical Industry: 3-anilinopropane-1,2-diol is used as an active pharmaceutical ingredient for its potential therapeutic effects. The presence of the anilino group may provide specific interactions with biological targets, making it a candidate for the development of new drugs. Used in Chemical Synthesis: In the chemical industry, 3-anilinopropane-1,2-diol can be used as a building block or intermediate in the synthesis of more complex organic compounds. The anilino group can be further modified or used as a starting point for the creation of various chemical products. Used in Material Science: 3-anilinopropane-1,2-diol may find applications in the development of new materials due to its unique chemical structure. The anilino group could potentially be utilized to create novel polymers or other materials with specific properties, such as improved conductivity or enhanced mechanical strength. Used in Research and Development: As a glycol derivative with a unique structure, 3-anilinopropane-1,2-diol can be employed in research and development for studying its properties and potential applications. This may include investigating its interactions with biological systems, its use in drug discovery, or its role in the synthesis of new compounds.

What is the CAS number for 3-anilinopropane-1,2-diol?

The CAS number of 3-anilinopropane-1,2-diol is 5840-15-3.

What is 3-anilinopropane-1,2-diol (5840-15-3) used for?

3-anilinopropane-1,2-diol, also known as ChEBI, is a glycol derivative of glycerol where one of the hydroxy groups is substituted by an anilino group. 3-anilinopropane-1,2-diol exhibits unique chemical properties due to the presence of the anilino group, which can potentially lead to various applications in different industries.InChI:InChI=1/C9H13NO2/c11-7-9(12)6-10-8-4-2-1-3-5-8/h1-5,9-12H,6-7H2

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3-anilinopropane-1,2-diol

CAS No.: 5840-15-3
Purity: 99%

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Manufacturers supply cost-effective and customizable 3-anilinopropane-1,2-diol 5840-15-3

Molecular Formula: C9H13 N O2
Molecular Weight: 167.208
Vapor Pressure: 1.33E-06mmHg at 25°C
Boiling Point: 384.6°Cat760mmHg
Flash Point: 194.5°C
PSA： 52.49000
Density: 1.217g/cm³
LogP: 0.52470

3-anilinopropane-1,2-diol(Cas 5840-15-3) Usage

Definition

ChEBI: A glycol that is a derivative of glycerol in which one of the hydroxy groups is replaced by an anilino group.

InChI:InChI=1/C9H13NO2/c11-7-9(12)6-10-8-4-2-1-3-5-8/h1-5,9-12H,6-7H2

5840-15-3 Relevant articles

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Bamberger,Kitschelt

, p. 3422 (1894)

Biotransformation of 3-(Phenylamino)-1,2-propanediol to 3-(Phenylamino)alanine: A Chemical Link between Toxic Oil Sindrome and Eosinophilia-Myalgia Syndrome

Mayeno, Arthur N.,Benson, Linda M.,Naylor, Stephen,Colberg-Beers, Marelisa,Puchalski, Jonathan T.,Gleich, Gerald J.

, p. 911 - 916 (1995)

During late 1989, the eosinophilia-myalg...

Catalytic synthesis of organic cyclic carbonate through CO2 fixation and production of β-amino alcohol via ring opening of epoxides under green condition by polystyrene embedded Al(III) catalyst

Biswas, Surajit,Roy, Dipanwita,Ghosh, Swarbhanu,Islam, Sk Manirul

, (2019/08/06)

Development of low cost, eco-friendly he...

A Multicomponent Approach to Oxazolidinone Synthesis Catalyzed by Rare-Earth Metal Amides

Zhou, Meixia,Zheng, Xizhou,Wang, Yaorong,Yuan, Dan,Yao, Yingming

, p. 5783 - 5787 (2019/04/14)

Three-component reaction of epoxides, am...

DISUBSTITUTED OXAZOLIDIN-2-ONES 5-HYDROXYTRYPTAMINE RECEPTOR 2B ACTIVITY MODULATORS

-

Paragraph 00216, (2014/06/23)

Pharmaceutical compositions of the inven...

The reaction of glycerol carbonate with primary aromatic amines in the presence of Y- and X-faujasites: The synthesis of N-(2,3-dihydroxy)propyl anilines and the reaction mechanism

Selva, Maurizio,Fabris, Massimo

experimental part, p. 1161 - 1172 (2010/05/18)

At 140 °C, in the presence of alkali met...

5840-15-3 Process route

: 556-52-5
oxiranyl-methanol

: 62-53-3
aniline

: 5840-15-3
1-phenylamino 2,3-propanediol

Conditions

Conditions	Yield
at 80 - 90 ℃; for 2h;	88%
In methanol; for 2.5h; Heating;	82%
at 80 - 90 ℃; for 2h;	76%
In methanol; at 50 - 60 ℃;	57%
at 90 ℃; for 2h;	8%

With polystyrene embedded aluminium(III) catalyst with 4-acetylpyridine thiosemicarbazone; at 20 ℃; for 3h; Green chemistry;