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2-[(1E)-2-nitroprop-1-en-1-yl]furan is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

134538-48-0

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134538-48-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 134538-48-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,5,3 and 8 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 134538-48:
(8*1)+(7*3)+(6*4)+(5*5)+(4*3)+(3*8)+(2*4)+(1*8)=130
130 % 10 = 0
So 134538-48-0 is a valid CAS Registry Number.

134538-48-0SDS

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 2-[(1E)-2-Nitro-1-propen-1-yl]fur

1.2 Other means of identification

Product number -
Other names o-Chlor-trans-propenylbenzol

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:134538-48-0 SDS

134538-48-0Relevant academic research and scientific papers

Guanidine-containing compound as well as preparation method and application thereof

-

Paragraph 0119-0122; 0129-0132, (2021/11/26)

The invention discloses a cyanoguanidine-containing compound as well as a preparation method and application thereof. The invention also discloses a composition containing the cyanoguanidine-structured compound (I) or a pharmaceutically acceptable salt thereof and a pharmaceutically acceptable carrier. The invention also discloses application thereof in preparation of analgesic drugs. The compounds of the invention are useful in the treatment of various pain.

Catalytic asymmetric Tamura cycloadditions involving nitroalkenes

Manoni, Francesco,Farid, Umar,Trujillo, Cristina,Connon, Stephen J.

, p. 1463 - 1474 (2017/02/15)

The first examples of asymmetric Tamura cycloaddition reactions involving singly activated alkenes are reported. Homophthalic anhydride reacts with α-methyl nitrosytrenes in the presence of an alkaloid-based catalyst to generate fused bicyclic aromatic ketone products with three new stereocentres (which are susceptible to subsequent equilibration) in 12-99% ee. An unusual equilibration process which occurs in methanolic medium in the absence of a recognisable base via proton transfer at the α-carbon of an ester was investigated experimentally and computationally.

Enantioselective hydrogenation of α,β-disubstituted nitroalkenes

Li, Shengkun,Huang, Kexuan,Zhang, Xumu

supporting information, p. 8878 - 8881 (2014/08/05)

The first highly chemo- and enantioselective hydrogenation of α,β-disubstituted nitroalkenes was accomplished with rhodium/JosiPhos-J2 as a catalyst, with the yield and enantioselectivity of up to 95% and 94%, respectively. The α-chiral nitroalkanes will provide an entry to valuable chiral amphetamines which are otherwise not so easily accessed. This journal is the Partner Organisations 2014.

Palladium-catalyzed synthesis of substituted nitroolefins

Chang, Meng-Yang,Lin, Chung-Han,Tai, Hang-Yi

supporting information, p. 3194 - 3198 (2013/06/26)

A one-pot protocol toward several substituted nitroolefins 4 and 6 starting with substituted acetones 2 and 5 was described. A facile process was carried out for the triflation of substituted acetones 2 and 5 with triflic anhydride (Tf2O) under the basic condition (Cs2CO3) and then palladium-catalyzed cross-coupling of enol triflates 3 with NaNO 2 and BINAP in the presence of phase-transfer reagents (n-Bu 4NBr) under the refluxing 1,2-dimethoxyethane (DME) in acceptable yields.

Alkenes from alcohols by tandem hydrogen transfer and condensation

Hall, Michael I.,Pridmore, Simon J.,Williams, Jonathan M. J.

supporting information; experimental part, p. 1975 - 1978 (2009/08/07)

A ruthenium-catalysed oxidation of alcohols by hydrogen transfer has been coupled with organocatalysed condensations using pyrrolidine or piperidine, to give α,β-unsaturated esters and nitroalkenes. Reactions proceed with high (E)-selectivity and provide an efficient and straightforward route to α,β-unsaturated compounds.

An efficient synthesis of (E)-nitroalkenes catalyzed by recoverable diamino-functionalized mesostructured polymers

Yan, Shaoyu,Gao, Yuan,Xing, Rong,Shen, Yali,Liu, Yueming,Wu, Peng,Wu, Haihong

, p. 6294 - 6299 (2008/09/21)

A clean, efficient, and simple method has been developed for synthesis of (E)-nitroalkenes using FDU-ED as an efficient catalyst. The reactions proceeded with moderate to high yields (60-96%) under mild conditions. The catalyst FDU-ED is recyclable and can be reused more than seven times without significant loss of activity and selectivity.

Heteroarylisopropylamines as MAO inhibitors

Vallejos, Gabriel,Fierro, Angelica,Rezende, Marcos Caroli,Sepulveda-Boza, Silvia,Reyes-Parada, Miguel

, p. 4450 - 4457 (2007/10/03)

The in vitro monoamine oxidase inhibitory (MAOI) activities of 11 heteroarylisopropylamines vis-a-vis MAO-A and MAO-B were described and interpreted in terms of possible interactions with the enzyme active site. Molecular dynamics simulations allowed a comparison between the most active MAO-A inhibitor of the series, the 1-(2-benzofuryl)-2-aminopropane, and the specific, analogous MAO-A substrate serotonin.

SiO2 Catalyzed Henry Reaction: Microwave Assisted Preparation of 2-Nitroalkanols in Dry Media

Kumar, H. M. Sampath,Reddy, B. V. Subba,Yadav, J. S.

, p. 637 - 638 (2007/10/03)

Nitroalkanes undergo rapid addition to aromatic aldehydes (Henry reaction) on the surface of activated SiO2, when irradiated with microwave, to afford 2-nitroalkanols in moderate to high yields.

HENRY CONDENSATION UNDER HIGH PRESSURE. 2. EFFECT OF AROMATIC ALDEHYDE TYPE AND PRESSURE ON THE YIELD OF ω-NITROSTYRENES AND SECONDARY PROCESSES

Agafonov, N. E.,Sedishev, I. P.,Dudin, A. V.,Kutin, A. A.,Stashina, G. A.,Zhulin, V. M.

, p. 366 - 372 (2007/10/02)

Condensation of aromatic aldehydes (I)-(XX) with EtNO2 and n-PrNO2 in AcOH in the presence of AcONH4 or i-BuNH2 gives primarily ω-nitrostyrenes (Ia, b) - (XXa, b) and small quantities of nitriles (Ic) - (XXc), oximes (Id) - (XXd), and ketones (Ie, f) - (XXe, f).The yields of (Ia, b) - (XXa, b) at P = 1 atm are higher for acceptor substitutents on the aromatic ring whereas at P = 10 kbar, they are higher for donor substituents.High pressures suppress the formation of (Ic-f) - (XXc-f) and the Z-isomers of (Ia, b) - (XXa, b).The high pressure technique is especially useful in the preparation of donor-substituted (Ia, b) - (XXa, b) which are intermediates in the synthesis of the psychotropic β-phenylethylamines.

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