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Benzyl 2-oxopropylcarbamate is a chemical compound that belongs to the class of organic compounds known as carbamates. Carbamates are organic compounds containing a functional group derived from carbamic acid. Although not much information is available about this specific chemical, similar chemicals in its group are used across various industries from medicine to agriculture. It is essential to handle them correctly and adhere to safety guidelines owing to their potential toxicity.

111491-97-5

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111491-97-5 Usage

Uses

Used in Pharmaceutical Industry:
Benzyl 2-oxopropylcarbamate is used as an intermediate compound for the synthesis of various pharmaceutical products. Its carbamate functional group allows it to be a versatile building block in the development of new drugs, potentially leading to the creation of novel therapeutic agents.
Used in Agricultural Industry:
Benzyl 2-oxopropylcarbamate is used as a pesticide or an ingredient in the formulation of agrochemicals. Its carbamate structure may provide it with insecticidal or herbicidal properties, making it a valuable component in the development of effective and environmentally friendly crop protection solutions.
Used in Chemical Research:
Benzyl 2-oxopropylcarbamate is used as a research compound in the field of organic chemistry. Its unique structure and properties make it an interesting subject for study, potentially leading to a better understanding of carbamate chemistry and the discovery of new applications in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 111491-97-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,4,9 and 1 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 111491-97:
(8*1)+(7*1)+(6*1)+(5*4)+(4*9)+(3*1)+(2*9)+(1*7)=105
105 % 10 = 5
So 111491-97-5 is a valid CAS Registry Number.

111491-97-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name Cbz-Gly-OH

1.2 Other means of identification

Product number -
Other names (2-oxopropyl)carbamic acid benzyl ester

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:111491-97-5 SDS

111491-97-5Relevant academic research and scientific papers

CHEMICAL COMPOUNDS

-

, (2020/06/01)

A compound of formula (I), wherein Ar1, R21, R23, R24, R25, R26, R27, A, X, Y and W are as defined herein. The compounds of the present invention are inhibitors of hematopoietic prostaglandin D synthase (H-PGDS) and can be useful in the treatment of Duchenne muscular dystrophy. Accordingly, the invention is further directed to pharmaceutical compositions comprising a compound of the invention. The invention is still further directed to methods of inhibiting H-PGDS activity and treatment of disorders associated therewith using a compound of the invention or a pharmaceutical composition comprising a compound of the invention.

Diarylpyrazole compound, composition containing the same and application thereof

-

, (2019/10/04)

The invention provides a diarylpyrazole compound, a composition containing the same and application thereof. The diarylpyrazole compound is the compound shown as formula (I) or its tautomer, stereisomer, prodrug, crystal form, pharmaceutically acceptable

A Straightforward Deracemization of sec-Alcohols Combining Organocatalytic Oxidation and Biocatalytic Reduction

Liardo, Elisa,Ríos-Lombardía, Nicolás,Morís, Francisco,González-Sabín, Javier,Rebolledo, Francisca

supporting information, p. 3031 - 3035 (2018/06/27)

An efficient organocatalytic oxidation of racemic secondary alcohols, mediated by sodium hypochlorite (NaOCl) and 2-azaadamantane N-oxyl (AZADO), has been conveniently coupled with a highly stereoselective bioreduction of the intermediate ketone, catalyzed by ketoreductases, in aqueous medium. The potential of this one-pot two-step deracemization process has been proven by a large set of structurally different secondary alcohols. Reactions were carried out up to 100 mm final concentration enabling the preparation of enantiopure alcohols with very high isolated yields (up to 98 %). When the protocol was applied to the stereoisomeric rac/meso mixture of diols, these were obtained with very high enantiomeric excesses and diastereomeric ratios (95 % yield, >99 % ee, >99: 1 dr).

NOVEL HIGH AFFINITY QUINOLINE-BASED KINASE LIGANDS

-

, (2014/01/09)

Quinoline-based inhibitors of cyclin dependent kinase 2, compositions including the inhibitors, and methods of using the inhibitors and inhibitor compositions are described. The inhibitors and compositions including them are useful for treating disease or disease symptoms. The invention also provides for methods of making CDK-2 inhibitor compounds, methods of inhibiting CDK-2, and methods for treating disease or disease symptoms.

Metallo-foldamers with backbone-coordinative oxime peptides: Control of secondary structures

Tashiro, Shohei,Matsuoka, Koji,Minoda, Ai,Shionoya, Mitsuhiko

supporting information, p. 13123 - 13127 (2013/02/26)

A new series of square-planar PdII-mediated foldamers with mononuclear and dinuclear helix or (double) hairpin structures were constructed by novel backbonecoordinative oxime peptides. Some of these metallo-foldamers allow significant structura

Catalyst-controlled Wacker-type oxidation of protected allylic amines

Michel, Brian W.,McCombs, Jessica R.,Winkler, Andrea,Sigman, Matthew S.

supporting information; experimental part, p. 7312 - 7315 (2010/11/05)

On the contrary: Utilizing the [Pd-(quinox)]-TBHP catalyst system, protected allylic amines were oxidized with high selectivity for the methyl ketone product. This is contrary to the results obtained by the substrate-controlled Tsuji-Wacker oxidation, which highlights the catalyst-controlled system presented here (see scheme). A variety of N-pro-tecting groups undergo selective oxidation with high ketone selectivity. TBHP = tert-butylhydroperoxide.

Reductive aldol and mannich-type reactions of azetidin-3-ones promoted by titanium tetraiodide

Hata, Shingo,Fukuda, Daisuke,Hachiya, Iwao,Shimizu, Makoto

supporting information; experimental part, p. 473 - 477 (2010/08/23)

A convenient method is described for the generation and reaction of the enolates of aminoacetone equivalents, which uses the reduction of azetidin-3-one with titanium tetraiodide and subsequent reactions with electrophiles. This methodology provides a str

Novel high affinity quinoline-based kinase ligands

-

Page/Page column 92, (2008/06/13)

Quinoline-based inhibitors of cyclin dependent kinase 2, compositions including the inhibitors, and methods of using the inhibitors and inhibitor compositions are described. The inhibitors and compositions including them are useful for treating disease or disease symptoms. The invention also provides for methods of making CDK-2 inhibitor compounds, methods of inhibiting CDK-2, and methods for treating disease or disease symptoms.

γ-Carboline derivatives with anti-bovine viral diarrhea virus (BVDV) activity

Sako, Kumiko,Aoyama, Hiroshi,Sato, Shinichi,Hashimoto, Yuichi,Baba, Masanori

, p. 3780 - 3790 (2008/12/20)

Based on anti-viral screening of our heteroaromatics derived from thalidomide, the γ-carboline skeleton has been identified as a superior scaffold structure for compounds with potent anti-bovine viral diarrhea virus (BVDV) activity. Structural development studies led to a potent anti-viral agent, SK5M (5-methyl-γ-carboline), with the EC50 of 0.26 μM.

Molecular transporter between polymer platforms: Highly efficient chemoenzymatic glycopeptide synthesis by the combined use of solid-phase and water-soluble polymer supports

Fumoto, Masataka,Hinou, Hiroshi,Matsushita, Takahiko,Kurogochi, Masaki,Ohta, Takashi,Ito, Takaomi,Yamada, Kuriko,Takimoto, Akio,Kondo, Hirosato,Inazu, Toshiyuki,Nishimura, Shin-Ichiro

, p. 2534 - 2537 (2007/10/03)

(Figure Presented) The molecule standing at platform one ...: Rapid glycopeptide synthesis is achieved with a heterobifunctional "molecular transporter" (see scheme), which interfaces two types of polymer platforms for combined chemical and enzymatic synt

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