75543-73-6

Basic information

• Product Name: 1,2-Propanediamine, 3-phenyl-
• Synonyms: 1,2-Propanediamine, 3-phenyl-
• CAS NO: 75543-73-6
• Molecular Formula: C₉H₁₄N₂
• Molecular Weight: 150.22
• Mol File: 75543-73-6.mol
• Article Data: 7

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1,2-Propanediamine, 3-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-Propanediamine, 3-phenyl-(75543-73-6)
• EPA Substance Registry System: 1,2-Propanediamine, 3-phenyl-(75543-73-6)

Safety Data

• Hazardous Substances Data: 75543-73-6(Hazardous Substances Data)

Usage

Diamine

Contains two amino (NH2) functional groups

Explanation

A diamine is a compound with two amino groups, which are characterized by the presence of a nitrogen atom bonded to two hydrogen atoms.

Explanation

The phenyl group is a functional group consisting of a six-carbon ring with alternating single and double bonds, which is attached to the second carbon atom in the amine chain.

Explanation

The compound's structure allows it to be used in the synthesis of a wide range of organic compounds, particularly those with pharmaceutical or biological applications.

Explanation

The compound can act as a reagent, which is a substance or compound that participates in a chemical reaction to produce a new substance.

Explanation

1,2-Propanediamine, 3-phenylcan be used as a starting material or building block in the synthesis of various polymers and other complex organic compounds.

Explanation

Due to its potential hazards and reactivity, special care should be taken when handling and using this compound to avoid accidents or adverse reactions.

Phenyl group

Presence of a six-carbon aromatic ring on the second carbon of the amine chain

Organic synthesis

Used as a building block for the production of various pharmaceuticals and biologically active molecules

Medicinal chemistry

Utilized in the development of new drugs and therapies

Reagent

Used in chemical reactions

Raw material

Used for the synthesis of polymers and other organic compounds

Hazards and reactivity

Must be handled and used with caution

Upstream product

• 93554-83-7 α-aminophenylpropiononitrile hydrochloride 
• 17193-31-6 (R,S)-2-amino-3-phenylpropionamide 
• 132653-51-1 2-benzyl-2-benzamidoethylamine 
• 113361-26-5 (E)-3-phenyl-1-nitroprop-1-ene 
• 5619-07-8 methyl 2-amino-3-phenylpropanoate hydrochloride 
• 114840-94-7 4-benzyl-1,3-dihydro-imidazol-2-one 
• 860259-19-4 1,3-diacetyl-4-benzyl-1,3-dihydro-imidazol-2-one 
• 55379-75-4 2-amino-3-phenylpropanenitrile 
• 7732-18-5 water 
• 65864-22-4 (S)-2-amino-3-phenylpropionamide hydrochloride 
• 5241-58-7 L-Phenylalanine amide 
• 63-91-2 L-phenylalanine 
• 7524-50-7 methyl (2S)-2-amino-3-phenylpropanoate hydrochloride 

Downstream Products

• 138036-51-8 1,2-diamino-N,N'-bis(2,2,2-trifluoro-1,1-diphenylethylsulfenyl)-3-phenylpropane 
• 64801-78-1 4⁽⁵⁾-Benzyl-2-mercaptoimidazoline 
• 128899-98-9 1,2-bis(N-isopropylamino)-3-phenylpropane 
• 64801-78-1 4-benzylimidazolidine-2-thione 

Relevant articles and documents

Method of making imidazole-2-thiones

The present invention provides a method of making an imidazole-2-thione which comprises the steps of reacting a vicinal diamine with a compound having a thiocarbonyl moiety and oxidizing the resulting reaction product to obtain said imidazole-2-thione.

Methods of preparing manganese complexes of nitrogen-containing macrocyclic ligands

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.

A new route to substituted-ethylenediamines

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