Production Method 1

74511-44-7

936497-77-7

Reaction Conditions

1.1 Reagents: Sodium bicarbonate ,  Hydroxyamine hydrochloride Solvents: Ethanol ;  6 h, reflux

Reference

Room-temperature synthesis of pharmaceutically important carboxylic acids bearing the 1,2,4-oxadiazole moiety

Tarasenko, Marina; Duderin, Nikolay; Sharonova, Tatyana; Baykov, Sergey ; Shetnev, Anton; et al, Tetrahedron Letters, 2017, 58(37), 3672-3677

Production Method 2

74511-44-7

936497-77-7

Reaction Conditions

1.1 Reagents: Sodium carbonate ,  Hydroxyamine hydrochloride Solvents: Ethanol ,  Water ;  20 h, rt → reflux

Reference

Fragment Growing to Design Optimized Inhibitors for Human Blood Group B Galactosyltransferase (GTB)

Strecker, Claas; Peters, Hannelore; Hackl, Thomas; Peters, Thomas; Meyer, Bernd, ChemMedChem, 2019, 14(14), 1336-1342

2-(Benzyloxy)-N'-hydroxybenzenecarboximidamide Raw materials

• 2-(benzyloxy)benzonitrile

2-(Benzyloxy)-N'-hydroxybenzenecarboximidamide Preparation Products

• 2-(Benzyloxy)-N'-hydroxybenzenecarboximidamide (936497-77-7)

• 1. Enabling non-flammable Li-metal batteries via electrolyte functionalization and interface engineering?
  Jing Yu,Yu-Qi Lyu,Jiapeng Liu,Mohammed B. Effat,Junxiong Wu J. Mater. Chem. A, 2019,7, 17995-18002
• 2. Evidence of field induced slow magnetic relaxation in cis-[Co(hfac)2(H2O)2] exhibiting tri-axial anisotropy with a negative axial component?
  Denis V. Korchagin,Elena A. Yureva,Alexander V. Akimov,Eugenii Ya. Misochko,Gennady V. Shilov,Artem D. Talantsev,Roman B. Morgunov,Alexander A. Shakin,Sergey M. Aldoshin,Boris S. Tsukerblat Dalton Trans., 2017,46, 7540-7548
• 3. Excellent lithium ion storage property of porous MnCo2O4 nanorods?
  Peiyuan Zeng,Xiaoxiao Wang,Ming Ye,Qiuyang Ma,Jianwen Li,Wanwan Wang,Baoyou Geng,Zhen Fang RSC Adv., 2016,6, 23074-23084
• 4. Ester-directed orthogonal dual C–H activation and ortho aryl C–H alkenylation via distal weak coordination?
  Manickam Bakthadoss,Tadiparthi Thirupathi Reddy,Vishal Agarwal,Duddu S. Sharada Chem. Commun., 2022,58, 1406-1409
• 5. Excitation dependent bidirectional electron transfer in phthalocyanine-functionalised MoS2 nanosheets?
  Christopher J. Harrison,Kyle J. Berean,Enrico Della Gaspera,Jian Zhen Ou,Richard B. Kaner,Kourosh Kalantar-zadeh,Torben Daeneke Nanoscale, 2016,8, 16276-16283

• Solvents and Organic Chemicals Organic Compounds Benzenoids Phenol ethers Phenol ethers
• Solvents and Organic Chemicals Organic Compounds Benzenoids Phenol ethers

2-(Benzyloxy)-N'-hydroxybenzenecarboximidamide (CAS No. 936497-77-7): A Comprehensive Overview

The compound 2-(Benzyloxy)-N'-hydroxybenzenecarboximidamide, identified by the CAS number 936497-77-7, is a highly specialized organic compound with significant potential in various fields of chemistry and materials science. This compound has garnered attention due to its unique structural properties and versatile applications. Recent advancements in synthetic methodologies and material characterization techniques have further highlighted its potential in drug delivery systems, electronic materials, and advanced polymers.

Recent studies have focused on the synthesis and characterization of 2-(Benzyloxy)-N'-hydroxybenzenecarboximidamide. Researchers have employed novel catalytic systems to optimize its synthesis, achieving higher yields and improved purity. The compound's structure, featuring a benzyloxy group and a hydroxylamine moiety, contributes to its unique reactivity and stability. These properties make it an ideal candidate for applications in medicinal chemistry, where precise control over molecular interactions is crucial.

In the context of materials science, 2-(Benzyloxy)-N'-hydroxybenzenecarboximidamide has been explored as a precursor for advanced polymers and self-healing materials. Its ability to form strong intermolecular hydrogen bonds has been leveraged to create materials with enhanced mechanical properties and thermal stability. Recent breakthroughs in polymer chemistry have demonstrated how this compound can be integrated into polymeric networks, leading to innovative materials for aerospace and automotive industries.

The pharmacological potential of 2-(Benzyloxy)-N'-hydroxybenzenecarboximidamide has also been a focal point of recent research. Preclinical studies suggest that it exhibits promising anti-inflammatory and antioxidant activities, making it a potential candidate for drug development. Its ability to modulate cellular signaling pathways has been extensively studied, with findings indicating potential applications in treating chronic inflammatory diseases.

Moreover, the environmental impact of synthesizing 2-(Benzyloxy)-N'-hydroxybenzenecarboximidamide has been a topic of interest. Green chemistry approaches have been implemented to minimize waste and reduce energy consumption during its production. These efforts align with global sustainability goals and highlight the importance of eco-friendly practices in modern chemical synthesis.

In conclusion, 2-(Benzyloxy)-N'-hydroxybenzenecarboximidamide (CAS No. 936497-77-7) stands as a testament to the advancements in organic chemistry and materials science. Its diverse applications, coupled with ongoing research into its properties, underscore its significance as a key compound in contemporary scientific exploration.

• 885957-55-1(3-ethoxy-N'-hydroxybenzene-1-carboximidamide)
• 771-28-8(2-Methoxybenzamidoxime)
• 90207-31-1(Benzenecarboximidamide,N-hydroxy-2,5-dimethoxy-)
• 62536-94-1(4-(Benzyloxy)-N'-hydroxybenzene-1-carboximidamide)
• 32048-12-7(2-Naphthalenecarboximidamide,6-(phenylmethoxy)-)
• 32152-42-4(Benzenecarboximidamide,4-[(2-naphthalenyloxy)methyl]-)
• 306936-07-2(2,3-Dihydrobenzobfuran-5-amidoxime)
• 145259-49-0(N'-hydroxy-4-propoxybenzenecarboximidamide)
• 57323-91-8(Benzenecarboximidamide, 3-[(2-naphthalenyloxy)methyl]-)
• 89446-97-9(Benzenecarboximidamide, 4,4'-oxybis[N-hydroxy-3-methyl-)