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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 articles and documents

PRODUCTION OF N-SUBSTITUTED AROMATIC HYDROXYLAMINE

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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.

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

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