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4-Pentenoic acid, 2-[(diphenylmethylene)amino]-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

80741-40-8

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80741-40-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 80741-40-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,7,4 and 1 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 80741-40:
(7*8)+(6*0)+(5*7)+(4*4)+(3*1)+(2*4)+(1*0)=118
118 % 10 = 8
So 80741-40-8 is a valid CAS Registry Number.

80741-40-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-(benzhydrylideneamino)pent-4-enoate

1.2 Other means of identification

Product number -
Other names ethyl N-(diphenylmethylene)-2-allylglycinate

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:80741-40-8 SDS

80741-40-8Relevant academic research and scientific papers

Catalytic Generation of Rhodium Silylenoid for Alkene-Alkyne-Silylene [2 + 2 + 1] Cycloaddition

Ohmura, Toshimichi,Sasaki, Ikuo,Suginome, Michinori

supporting information, p. 1649 - 1653 (2019/03/20)

An alkene-alkyne-silylene [2 + 2 + 1] cycloaddition takes place in the rhodium-catalyzed reaction of 1,6-enynes with borylsilanes bearing an alkoxy group on the silicon atoms, which react as synthetic equivalents of silylene. The reaction proceeds efficiently in 1,2-dichloroethane at 80-110 °C in the presence of a rhodium catalyst bearing bis(diphenylphosphino)methane (DPPM) as a ligand to afford 1-silacyclopent-2-enes in good to high yields.

Lewis acidic FeCl3 promoted 2-aza-Cope rearrangement to afford α-substituted homoallylamines in dimethyl carbonate

Gadde, Karthik,Daelemans, Jonas,Maes, Bert U. W.,Abbaspour Tehrani, Kourosch

, p. 18013 - 18017 (2019/06/24)

The iron(iii)-catalyzed efficient strategy for the synthesis of α-substituted homoallylamines was accomplished via a cationic 2-aza-Cope rearrangement of aldimines, generated in situ by condensation of commercially available aldehydes and easily synthesizable 1,1-diphenylhomoallylamines. This reaction features a broad substrate scope with high yields and is conducted in an eco-friendly solvent, i.e. dimethyl carbonate.

Arginase Inhibitors and Their Therapeutic Applications

-

Paragraph 1091; 1092; 1093, (2017/11/29)

Disclosed are small molecule therapeutic compounds that are potent inhibitors of arginase 1 and arginase 2 activity. Also disclosed are pharmaceutical compositions comprising the compounds, and methods for using the compounds for treating or preventing a

Iron-catalyzed oxidative C - H/C - H cross-coupling: An efficient route to α-quaternary α-amino acid derivatives

Li, Kaizhi,Tan, Guangying,Huang, Jingsheng,Song, Feijie,You, Jingsong

supporting information, p. 12942 - 12945 (2014/01/06)

Fully loaded: A coordinating activation strategy has been developed to furnish α-quaternary α-amino acids through the iron(III)-catalyzed oxidative functionalization of α-C(sp3) - H bonds of α-tertiary α-amino acid esters. The reaction exhibits a broad substrate scope for both α-amino acids and nucleophiles (Nu) as well as good functional-group tolerance (see scheme, DTBP=di-tert-butyl peroxide, DCE=1,2-dichloroethane). Copyright

The synthesis and characterization of a pentafluorosulfanylated peptide

Lim, Dong Sung,Lin, Jin-Hong,Welch, John T.

experimental part, p. 3946 - 3954 (2012/08/28)

The design and synthesis of pentafluorosulfanyl-containing heptad amino acid sequence was described. The three-dimensional conformation of the peptide was investigated by using CYANA (combined assignment and dynamics algorithm for NMR applications) and th

PENTAFLUOROSULFANYL CONTAINING AMINO ACIDS

-

Page/Page column 12, (2008/12/08)

There are provided SF5-containing amino acids of general formulas (I), (II), (III) and processes for preparing same. Other embodiments are also disclosed.

HCV PROTEASE INHIBITORS

-

Page/Page column 23, (2008/12/07)

This invention relates to the compounds of formula (I) shown below. Each variable in formula (I) is defined in the specification. These compounds can be used to treat hepatitis C virus infection.

C-C bond-forming reactions via Pd-mediated decarboxylative α-lmino anion generation

Yeagley, Andrew A.,Chruma, Jason J.

, p. 2879 - 2882 (2008/02/07)

α-lmino anions are generated under neutral reaction conditions via a Pd-mediated decarboxylation of allyl diphenylglycinate imines with concomitant formation of a π-allylpalladium species. The resulting delocalized anion can attack the π-allyl-Pd(ll) spec

A new synthetic approach to 1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid (Tic) derivatives via enyne metathesis and the Diels-Alder reaction

Kotha, Sambasivarao,Sreenivasachary, Nampally

, p. 503 - 504 (2007/10/03)

Various substituted 1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid (Tic) derivatives are synthesized via enyne metathesis and the Diels-Alder reaction.

Easy and efficient generation of reactive anions with free and supported ylides as neutral Bronsted bases

Palacios, Francisco,Aparicio, Domitila,De Los Santos, Jesús M.,Baceiredo, Antoine,Bertrand, Guy

, p. 663 - 669 (2007/10/03)

The tris(dimethylamino)-C-dimethylphosphorus ylide 5 and the tris(dimethylamino)phosphorus ylide C-bound to Merrifield's resin 6 are used as strong non-nucleophilic bases in N-alkylation reactions of β-amino phosphine oxides and α-amino acid derivatives,

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