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(2E)-2-[(3-nitrophenyl)methylidene]-1-benzofuran-3(2H)-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

70170-87-5

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70170-87-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 70170-87-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,1,7 and 0 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 70170-87:
(7*7)+(6*0)+(5*1)+(4*7)+(3*0)+(2*8)+(1*7)=105
105 % 10 = 5
So 70170-87-5 is a valid CAS Registry Number.

70170-87-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (2E)-2-[(3-nitrophenyl)methylidene]-1-benzofuran-3-one

1.2 Other means of identification

Product number -
Other names 3(2H)-Benzofuranone,2-((3-nitrophenyl)methylene)

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:70170-87-5 SDS

70170-87-5Downstream Products

70170-87-5Relevant academic research and scientific papers

Synthesis of some modified aurones as antileukemic and antibacterial agents

Deepthi,Harinadha, Babu V,Madhava, Reddy B

, p. 1455 - 1461 (2014/01/06)

Cyclisation of 1-(2-hydroxyphenyl)-3-substituted phenylprop-2-en-1-ones 1a-h in pyridine with mercuric acetate gives different 2-benzylidene-1- benzofuran-3(2H)-ones 2a-h which on subsequent reaction with hydroxylamine hydrochloride affords 2-benzylidene-

Amine-effected cyclization of chalcone dihalides to aurones

Donnelly, John A.,Emerson, Geraldine M.

, p. 7227 - 7236 (2007/10/02)

The possibility of employing the amine-catalysed cyclization of αβ-dibromodihydrochalcones and α-bromochalcones as a general synthesis of aurones was studied using cyclohexylamine and the most representative member of each class of these αβ-disubstituted ketones and α-halogeno chalcones. Overall yields of heterocyclic products were generally poor except from 4′6′-dimethoxy- and 3-nitro-substituted chalcone systems; aurones were obtained in fair yield from the former and in excellent yield from the latter. 22′-Diacetoxychalcone dibromide and 22′-diacetoxy-α-bromochalcone cyclised to a 2-benzoylbenzofuran to the exclusion of the corresponding aurone and flavone.

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