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Carbamic acid, hydroxyphenyl-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

28091-62-5

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28091-62-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 28091-62-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,0,9 and 1 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 28091-62:
(7*2)+(6*8)+(5*0)+(4*9)+(3*1)+(2*6)+(1*2)=115
115 % 10 = 5
So 28091-62-5 is a valid CAS Registry Number.

28091-62-5SDS

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 methyl N-hydroxy-N-phenylcarbamate

1.2 Other means of identification

Product number -
Other names C-methoxy-N-phenylhydroxamic acid

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:28091-62-5 SDS

28091-62-5Relevant academic research and scientific papers

PRODUCTION OF N-SUBSTITUTED AROMATIC HYDROXYLAMINE

-

Paragraph 0047-0048, (2020/01/12)

An economic, one-step method for the production of N-substituted aromatic hydroxylamines of formula (I) [in-line-formulae]R—N(OH)—C(═O)—(O)R1??(I),[/in-line-formulae] with hydrogen, by catalytic hydration with possibly modified hydration catalysts in an aprotic solvent and in the presence of a halogen formic acid ester and in some cases in the presence of a base.

Copper-Catalyzed Aerobic Decarboxylation/Ketooxygenation of Electron-Deficient Alkenes

Lu, Qingquan,Peng, Pan,Luo, Yi,Zhao, Ying,Zhou, Minxian,Lei, Aiwen

supporting information, p. 18580 - 18583 (2016/01/25)

A copper-catalyzed ketooxygenation of electron-deficient alkenes was developed. This approach combines O-H alkylation, aerobic decarboxylation, and oxygenation in one transformation. Mechanistic investigation of this reaction showed that the copper salt is responsible for both generating the amidoxyl radical and promoting aerobic decarboxylation.

Metal-free, aerobic dioxygenation of alkenes using simple hydroxamic acid derivatives

Giglio, Benjamin C.,Schmidt, Valerie A.,Alexanian, Erik J.

supporting information; experimental part, p. 13320 - 13322 (2011/10/10)

The dioxygenation of alkenes using molecular oxygen and a simple hydroxamic acid derivative has been achieved. The reaction system consists of readily prepared methyl N-hydroxy-N-phenylcarbamate and molecular oxygen with a radical initiator, offering an alternative to common dioxygenation processes catalyzed by precious transition metals. This transformation capitalizes on the unique reactivity profile of hydroxamic acid derivatives in radical-mediated alkene addition processes.

Laccase Variants

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, (2011/05/03)

The present invention relates to variants of a parent laccase. The present invention also relates to polynucleotides encoding the variant laccases and to nucleic acid constructs, vectors, and host cells comprising the polynucleotides, and methods of using the variant enzymes.

Facile procedure for the synthesis of N-aryl-N-hydroxy carbamates

Porzelle, Achim,Woodrow, Michael D.,Tomkinson, Nicholas C. O.

experimental part, p. 798 - 802 (2009/07/25)

An efficient one-pot procedure for the zinc-mediated reduction of nitroarenes in the presence of chloroformates leading to the corresponding N,O-bisprotected hydroxylamine is described. Reactions proceed smoothly under ambient conditions in THF-water mixt

ANTIMICROBIAL COMPOSITION CONTAINING AN OXIDOREDUCTASE AND AN ENHANCER OF THER N-HYDROXYANILIDE-TYPE

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, (2008/06/13)

The present invention relates to an enzymatic composition capable of killing or inhibiting microbial cells or micro-organisms, e.g. in laundry, on hard surfaces, in water systems, on skin, on teeth or on mucous membranes. The present invention also relate

A formal synthesis of (±)-eseroline via an azaoxy-cope rearrangement

Santos, Paulo F.,Almeida, Paulo S.,Lobo, Ana M.,Prabhakar, Sundaresan

, p. 1029 - 1043 (2007/10/03)

A novel synthesis of (±)-desoxyeseroline, from the crucial oxindole (15), obtained by a 3,3-sigmatropic rearrangement of the enolate derived from the hydroxamic acid derivative (5) followed by radical desulfurisation, has been described. The requisite Cs

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