74974-49-5

Basic information

• Product Name: [4-(DIETHYLAMINO)PHENYL]METHANOL
• Synonyms: [4-(DIETHYLAMINO)PHENYL]METHANOL;RARECHEM AL BD 0080;AKOS BBV-004765;ASISCHEM V82751;UKRORGSYN-BB BBV-004765
• CAS NO: 74974-49-5
• Molecular Formula: C₁₁H₁₇NO
• Molecular Weight: 179.26
• Mol File: 74974-49-5.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 305.4°Cat760mmHg
• Flash Point: 145.4°C
• Appearance: /
• Density: 1.028g/cm³
• Vapor Pressure: 0.000359mmHg at 25°C
• Refractive Index: 1.559
• CAS DataBase Reference: [4-(DIETHYLAMINO)PHENYL]METHANOL(CAS DataBase Reference)
• NIST Chemistry Reference: [4-(DIETHYLAMINO)PHENYL]METHANOL(74974-49-5)
• EPA Substance Registry System: [4-(DIETHYLAMINO)PHENYL]METHANOL(74974-49-5)

Safety Data

• Hazardous Substances Data: 74974-49-5(Hazardous Substances Data)

Usage

General Description

[4-(diethylamino)phenyl]methanol is a chemical compound with the molecular formula C13H19NO. It is a white to light yellow solid that is classified as a tertiary amine and an aromatic alcohol. It is commonly used as an intermediate in the synthesis of pharmaceuticals, dyes, and other organic compounds. The compound is also known for its potential as a strong base and nucleophile, making it useful in various chemical reactions. Additionally, [4-(diethylamino)phenyl]methanol is known to exhibit some pharmacological properties, which has led to research on its potential use as a therapeutic agent or as a chemical probe in biological studies. Overall, it is a versatile compound with various potential applications in the field of chemistry and pharmacology.

InChI:InChI=1/C11H17NO/c1-3-12(4-2)11-7-5-10(9-13)6-8-11/h5-8,13H,3-4,9H2,1-2H3

Upstream product

• 50-00-0 formaldehyd 
• 91-66-7 N,N-diethylaniline 
• 459-57-4 4-fluorobenzaldehyde 
• 120-21-8 4-Diethylaminobenzaldehyde 
• 7647-01-0 hydrogenchloride 

Downstream Products

• 143627-57-0 [4-(2-Amino-ethylsulfanylmethyl)-phenyl]-diethyl-amine 
• 940362-30-1 N,N-diethyl-4-((phenylamino)methyl)aniline 
• 613-48-9 N,N-diethyl-p-toluidine 
• 120-21-8 4-Diethylaminobenzaldehyde 
• 1273324-91-6 (E)-4-(4-thiostyryl)-N,N-diethylbenzenamine 
• 1273324-90-5 (E)-4-(4-(tert-butylthio)styryl)-N,N-diethylbenzenamine 
• 1283742-12-0 (E)-4-(4-(benzylthio)styryl)-N,N-diethylbenzenamine 
• 143627-73-0 N-Benzoyl-N'-[2-(4-diethylamino-benzylsulfanyl)-ethyl]-N''-[3-(1H-imidazol-4-yl)-propyl]-guanidine 
• 932714-76-6 1-[trans-4-(4-diethylaminostyryl)phenyl]imidazole 
• 5429-28-7 4-(diethylamino)benzoic acid 

Relevant articles and documents

Transfer Hydrogenation of Carbonyl Derivatives Catalyzed by an Inexpensive Phosphine-Free Manganese Precatalyst

A very simple and inexpensive catalytic system based on abundant manganese as transition metal and on an inexpensive phosphine-free bidendate ligand, 2-(aminomethyl)pyridine, has been developed for the reduction of a large variety of carbonyl derivatives with 2-propanol as hydrogen donor. Remarkably, the reaction proceeds at room temperature with low catalyst loading (down to 0.1 mol %) and exhibits a good tolerance toward functional groups. High TON (2000) and TOF (3600 h-1) were obtained.

Three asymmetrical conjugated D-π-D′ sulfur-containing chromophores with a focus on two-photon absorption

Three novel asymmetrical D-π-D′ type sulfur-containing chromophores, (E)-4-(4-(benzylthio)styryl)-N,N-diethylbenzenamine (S1), (E)-4-(4-(tert-butylthio)styryl)-N,N-diethylbenzenamine (S2) and (E)-4-(4-(thio)styryl)-N,N-diethylbenzenamine (S3), were synthe

Synthesis, crystal structures, and optical properties of a novel imidazole derivative and its Zn(II) complex

A novel imidazole derivative, 1-[trans-4-(4-diethylaminostyryl)phenyl]imidazole (abbreviated as L), and its complex Zn(SCN)2L2 have been synthesized and fully characterized. Their crystal structures have been determined by X-ray diffraction. The molecular structure of L is approximately coplanar, the bond lengths of C-C and C-N are located between the normal double and single bonds, which show that L has a delocalized π-electron system in the molecule. In the molecular structure of Zn(SCN)2L2, zinc atom is four coordinated by two nitrogen atoms of the ligands (L) and two nitrogen atoms of thiocyanate to form a distorted tetrahedral geometry. The one-dimensional structure of Zn(SCN)2L2 is formed by C-H?S interactions and π-π interactions. They both crystallize in the noncentrosymmetric space group P21, and exhibit powder second-harmonic generation (SHG) efficiency approximately twenty times high as that of urea, indicating promising potential applications as useful nonlinear optical (NLO) materials.