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O-Benzylhydroxylamine is an organic compound with the chemical formula C6H5CH2NOH. It is a clear colorless liquid and is commonly used as a reagent in the synthesis of various organic compounds.

622-33-3

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622-33-3 Usage

Uses

1. Used in Pharmaceutical Industry:
O-Benzylhydroxylamine is used as a synthetic reagent for the preparation of α-hydroxybenzylamines from α-hydroxyketones. This application is significant in the development of new pharmaceutical compounds with potential therapeutic properties.
2. Used in Chemical Synthesis:
O-Benzylhydroxylamine is used as a reagent in the preparation of hydroxylamines and hydroxyamates. These compounds are essential intermediates in the synthesis of various organic molecules, including those with applications in the chemical, pharmaceutical, and materials science industries.

Check Digit Verification of cas no

The CAS Registry Mumber 622-33-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,2 and 2 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 622-33:
(5*6)+(4*2)+(3*2)+(2*3)+(1*3)=53
53 % 10 = 3
So 622-33-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H9NO/c8-9-6-7-4-2-1-3-5-7/h1-5H,6,8H2

622-33-3 Well-known Company Product Price

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  • Alfa Aesar

  • (L13601)  O-Benzylhydroxylamine, 96%   

  • 622-33-3

  • 5g

  • 611.0CNY

  • Detail
  • Alfa Aesar

  • (L13601)  O-Benzylhydroxylamine, 96%   

  • 622-33-3

  • 25g

  • 2337.0CNY

  • Detail

622-33-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name O-Benzylhydroxylamine

1.2 Other means of identification

Product number -
Other names Benzyl-O-Hydroxylamine

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:622-33-3 SDS

622-33-3Relevant academic research and scientific papers

A Pictet-Spengler ligation for protein chemical modification

Agarwal, Paresh,Van Der Weijden, Joep,Sletten, Ellen M.,Rabuka, David,Bertozzi, Carolyn R.

, p. 46 - 51 (2013)

Aldehyde- and ketone-functionalized proteins are appealing substrates for the development of chemically modified biotherapeutics and protein-based materials. Their reactive carbonyl groups are typically conjugated with α-effect nucleophiles, such as substituted hydrazines and alkoxyamines, to generate hydrazones and oximes, respectively. However, the resulting C=N linkages are susceptible to hydrolysis under physiologically relevant conditions, which limits the utility of such conjugates in biological systems. Here we introduce a Pictet-Spengler ligation that is based on the classic Pictet- Spengler reaction of aldehydes and tryptamine nucleophiles. The ligation exploits the bioorthogonal reaction of aldehydes and alkoxyamines to form an intermediate oxyiminium ion; this intermediate undergoes intramolecular C-C bond formation with an indole nucleophile to form an oxacarboline product that is hydrolytically stable. We used the reaction for site-specific chemical modification of glyoxyl- and formylglycine-functionalized proteins, including an aldehyde-tagged variant of the therapeutic monoclonal antibody Herceptin. In conjunction with techniques for site-specific introduction of aldehydes into proteins, the Pictet-Spengler ligation offers a means to generate stable bioconjugates for medical and materials applications.

Oxime ether heterocyclic formamide derivatives and preparation method and application thereof

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Paragraph 0064-0066, (2021/02/13)

The invention provides an oxime ether heterocyclic formamide derivative and a preparation method and application thereof, and particularly relates to the oxime ether heterocyclic formamide derivativeof which the chemical structural general formula is shown in a formula I. The invention discloses the structural general formula, a synthesis method and an application of the oxime ether heterocyclicformamide derivative serving as an insecticide, a bactericide and a plant virus resisting agent. The invention also discloses an application of the insecticidal composition in preventing and treatingagricultural, forestry and horticultural plant insect pests, diseases and virus diseases in combination with agriculturally acceptable auxiliaries or synergists and commercial insecticides, bactericides, plant virus resisting agents and acaricides, and a preparation method of the insecticidal composition in prevention and treatment of agricultural, forestry and horticultural plant insect pests, diseases and virus diseases.

Vinylogous Aza-Michael Addition of Urea Derivatives with p-Quinone Methides Followed by Oxidative Dearomative Cyclization: Approach to Spiroimidazolidinone Derivatives

Kaur, Navpreet,Singh, Priyanka,Banerjee, Prabal

supporting information, p. 2813 - 2824 (2021/04/21)

Herein, we report an efficient protocol for the synthesis of spiro-imidazolidinone-cyclohexadienones from p-quinone methides (p-QMs) and dialkyloxy ureas under mild conditions. The strategy follows a two-step process involving an initial vinylogous conjugate addition of urea derivatives to p-QMs, followed by oxidative dearomative cyclization of open-chain product to the projected spiro-imidazolidinones. This protocol exhibits good functional group tolerance and provides a straightforward method to access spiro-imidazolidinone-cyclohexadienones. In follow-up chemistry, we have shown the debenzylation of spiroimidazolidinones to give N-hydroxycyclic ureas. (Figure presented.).

Synthesis, Crystal Structure, Herbicidal Activity, and SAR Study of Novel N-(Arylmethoxy)-2-chloronicotinamides Derived from Nicotinic Acid

Yu, Chen-Sheng,Wang, Qiao,Bajsa-Hirschel, Joanna,Cantrell, Charles L.,Duke, Stephen O.,Liu, Xing-Hai

, p. 6423 - 6430 (2021/06/28)

Nicotinic acid, also known as niacin, is a natural product, which is widely found in plants and animals. To discover novel natural-product-based herbicides, a series of N-(arylmethoxy)-2-chloronicotinamides were designed and synthesized. Some of the new N-(arylmethoxy)-2-chloronicotinamides exhibited excellent herbicidal activity against Agrostis stolonifera (bentgrass) at 100 μM. Compound 5f (2-chloro-N-((3,4-dichlorobenzyl)oxy)nicotinamide) possessed excellent herbicidal activity against Lemna paucicostata (duckweed), with an IC50 value of 7.8 μM, whereas the commercial herbicides clomazone and propanil had values of 125 and 2 μM, respectively. The structure-activity relationships reported in this paper could be used for the development of new herbicides against monocotyledonous weeds.

N-(benzyloxy)-2-chloronicotinamide compound as well as preparation method and application thereof

-

Paragraph 0016; 0037-0038, (2021/06/23)

The invention belongs to the technical field of chemical synthesis and medicine application, and particularly relates to preparation and application of an N-(benzyloxy)-2-chloronicotinamide compound. The preparation method comprises the following steps: reacting phthalic anhydride with hydroxylamine, then reacting with triethylamine for acidification to prepare N-hydroxyphthalimide, then carrying out substitution and hydrazinolysis, and finally reacting with dichloronicotinoyl chloride to prepare the N-(benzyloxy)-2-chloronicotinamide compound. The preparation method disclosed by the invention is simple and convenient to operate, the structure of the obtained product is confirmed by a nuclear magnetic hydrogen spectrum, herbicidal activity tests are carried out on the obtained 15 target products, and results show that all target compounds have an obvious inhibition effect on the seeds of the Agrostis matsumurae under the concentration of 1mM, and the inhibition effect reaches 100%; and along with the decrease of the concentration, even if the concentration reaches 100 [mu] M, the target compound can still show good herbicidal activity.

Novel fluorinated 7-hydroxycoumarin derivatives containing an oxime ether moiety: Design, synthesis, crystal structure and biological evaluation

Dai, Peng,Jiao, Jian,Wang, Qing-Qing,Zhang, Shu-Guang,Zhang, Wei-Hua

, (2021/06/28)

A series of fluorinated 7-hydroxycoumarin derivatives containing an oxime ether moiety have been designed, synthesized and evaluated for their antifungal activity. All the target compounds were determined by1H-NMR,13C-NMR, FTIR and HR-MS spectra. The single-crystal structures of compounds 4e, 4h, 5h and 6c were further confirmed using X-ray diffraction. The antifungal activities against Botrytis cinerea (B. cinerea), Alternaria solani (A. solani), Gibberella zeae (G. zeae), Rhizoctorzia solani (R. solani), Colletotrichum orbiculare (C. orbiculare) and Alternaria alternata (A. alternata) were evaluated in vitro. The preliminary bioassays showed that some of the designed compounds displayed the promising antifungal activities against the above tested fungi. Strikingly, the target compounds 5f and 6h exhibited outstanding antifungal activity against B. cinerea at 100 μg/mL, with the corresponding inhibition rates reached 90.1 and 85.0%, which were better than the positive control Osthole (83.6%) and Azoxystrobin (46.5%). The compound 5f was identified as the promising fungicide candidate against B. cinerea with the EC50 values of 5.75 μg/mL, which was obviously better than Osthole (33.20 μg/mL) and Azoxystrobin (64.95 μg/mL). Meanwhile, the compound 5f showed remarkable antifungal activities against R. solani with the EC50 values of 28.96 μg/mL, which was better than Osthole (67.18 μg/mL) and equivalent to Azoxystrobin (21.34 μg/mL). The results provide a significant foundation for the search of novel fluorinated 7-hydroxycoumarin derivatives with good antifungal activity.

N-benzyloxy substituted symmetric oxamide compound and preparation method and application thereof

-

Paragraph 0031; 0033-0034, (2020/12/30)

The invention discloses an N-benzyloxy substituted symmetric oxamide compound and a preparation method and application thereof, the structural formula of the N-benzyloxy substituted symmetric oxamidecompound is shown as the formula (I): in the formula (I), the structures of two substituted benzene rings are the same, the number of substituents R on each substituted benzene ring is 1-2, and the substituent R is selected from H, halogen, C1-C4 alkyl or C1-C3 alkoxy. The N-benzyloxy substituted symmetric oxamide compound is a new compound with an efficient weeding effect, and provides a basis for research and development of a novel herbicide.

Hydrogen-Bond Catalysis of Imine Exchange in Dynamic Covalent Systems

Schaufelberger, Fredrik,Seigel, Karolina,Ramstr?m, Olof

, p. 15581 - 15588 (2020/10/02)

The reversibility of imine bonds has been exploited to great effect in the field of dynamic covalent chemistry, with applications such as preparation of functional systems, dynamic materials, molecular machines, and covalent organic frameworks. However, acid catalysis is commonly needed for efficient equilibration of imine mixtures. Herein, it is demonstrated that hydrogen bond donors such as thioureas and squaramides can catalyze the equilibration of dynamic imine systems under unprecedentedly mild conditions. Catalysis occurs in a range of solvents and in the presence of many sensitive additives, showing moderate to good rate accelerations for both imine metathesis and transimination with amines, hydrazines, and hydroxylamines. Furthermore, the catalyst proved simple to immobilize, introducing both reusability and extended control of the equilibration process.

NOVEL ALKENYL AND BETA-SUBSTITUTED PHOSPHONATES AS ANTIMICROBIAL AGENTS

-

Paragraph 0191; 0156, (2019/01/17)

The present disclosure relates to novel compounds, pharmaceutical compositions, and methods for treating or preventing microbial infection caused by parasites or bacteria, such as Plasmodium falciparum or related Plasmodium parasite species and Mycobacterium tuberculosis or related Mycobacterium bacteria species. The compounds are α,β-unsaturated analogs of fosmidomycin and can inhibit deoxyxylulose phosphate reductoisomerase (Dxr) in many microbes, such as P. falciparum.

Catalytic asymmetric aza-Michael addition of fumaric monoacids with multifunctional thiourea/boronic acids

Michigami, Kenichi,Murakami, Hiroki,Nakamura, Takeru,Hayama, Noboru,Takemoto, Yoshiji

supporting information, p. 2331 - 2335 (2019/03/06)

The first chemical enantioselective synthesis of N-hydroxyaspartic acid derivatives using chiral multifunctional thiourea/boronic acid organocatalysts was developed. A series of fumaric monoacids underwent an intermolecular asymmetric aza-Michael addition of O-alkyl hydroxylamines in excellent regioselectivity. The addition of another carboxylic acid raised the enantiomeric enrichment up to 97% ee. O-Deprotection of the aza-Michael adduct provided an aspartate-derived hydroxylamine fragment applicable for KAHA (α-keto acid-hydroxylamine) ligation.

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