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114570-69-3

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114570-69-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 114570-69-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,5,7 and 0 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 114570-69:
(8*1)+(7*1)+(6*4)+(5*5)+(4*7)+(3*0)+(2*6)+(1*9)=113
113 % 10 = 3
So 114570-69-3 is a valid CAS Registry Number.

114570-69-3SDS

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 3-(2-furyl)-1-(4-methoxyphenyl)propen-1-one

1.2 Other means of identification

Product number -
Other names .1-[Furyl-(2)]-3-[4-methoxy-phenyl]-propen-(1)-on-(3)

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:114570-69-3 SDS

114570-69-3Relevant articles and documents

Regiospecific Aza-Michael Addition of 4-Aryl-1 H -1,2,3-triazoles to Chalcones: Synthesis of 2,4-Disubstituted 1,2,3-Triazoles in Basic Medium

Bhagat, Ujjawal Kumar,Peddinti, Rama Krishna

, p. 99 - 105 (2018)

A novel metal-free and base-mediated method to display the donor ability of 1,2,3-triazoles for the synthesis of 2,4-disubstituted 1,2,3-triazoles has been developed. A DABCO-promoted aza-Michael addition of 4-aryl NH-1,2,3-triazoles to α,β-unsaturated ketones (chalcones) is presented. The reactions proceeded with complete regiospecificity in a 3:1 mixture of acetonitrile and methanol at 85 °C to provide 2,4-disubstituted 1,2,3-triazoles as Michael adducts, and the addition products 1,3-diaryl-(4-aryl-2 H -1,2,3-triazol-2-yl)propan-1-ones were isolated in high yields.

Design, synthesis, topoisomerase I & II inhibitory activity, antiproliferative activity, and structure-activity relationship study of pyrazoline derivatives: An ATP-competitive human topoisomerase IIα catalytic inhibitor

Ahmad, Pervez,Woo, Hyunjung,Jun, Kyu-Yeon,Kadi, Adnan A.,Abdel-Aziz, Hatem A.,Kwon, Youngjoo,Rahman, A.F.M. Motiur

, p. 1898 - 1908 (2016)

A series of pyrazoline derivatives (5) were synthesized in 92-96% yields from chalcones (3) and hydrazides (4). Subsequently, topo-I and IIα-mediated relaxation and antiproliferative activity assays were evaluated for 5. Among the tested compounds, 5h had

Design, synthesis, and antifungal activity evaluation of novel 2-cyano-5-oxopentanoic acid derivatives as potential succinate dehydrogenase inhibitors

Mai, Yong-zhan,Peng, Mi-jun,Tang, Xiao-rong,Wang, Xue-song

, p. 94 - 107 (2021/11/22)

Two series of novel 2-cyano-5-oxopentanoic acid derivatives (1a?l, 2a?l) were designed, synthesized, and characterized by IR, 1H NMR, 13C NMR, and HRMS. Their in vitro antifungal activity against five plant pathogenic fungi were then

N-(4-fluorophenyl)-4,5-dihydropyrazole compounds and application thereof in farm chemicals

-

Paragraph 0055-0057, (2020/05/01)

The invention relates to N-(4-fluorophenyl)-4,5-dihydropyrazole compounds and application thereof in farm chemicals, and belongs to the technical field of farm chemicals. The technical problem solvedby the present invention is to provide novel compounds t

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