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79017-08-6

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79017-08-6 Usage

Uses

3-(1-Nitroethyl)-2-benzofuran-1(3H)-one can be used as an antihypertensive.

Check Digit Verification of cas no

The CAS Registry Mumber 79017-08-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,0,1 and 7 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 79017-08:
(7*7)+(6*9)+(5*0)+(4*1)+(3*7)+(2*0)+(1*8)=136
136 % 10 = 6
So 79017-08-6 is a valid CAS Registry Number.
InChI:InChI=1/C10H9NO4/c1-6(11(13)14)9-7-4-2-3-5-8(7)10(12)15-9/h2-6,9H,1H3/t6-,9+/m1/s1

79017-08-6SDS

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 3-(1-nitroethyl)-3H-2-benzofuran-1-one

1.2 Other means of identification

Product number -
Other names 3-(1-nitroethyl)isobenzofuran-1(3H)-one

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:79017-08-6 SDS

79017-08-6Relevant articles and documents

Active methylene compounds in a very effective approach to 3-substituted isobenzofuranones through tandem aldol/lactonization reactions

Di Mola, Antonia,Croce, Gianluca,More, Vijaykumar,De Caprariis, Paolo,Filosa, Rosanna,Massa, Antonio

experimental part, p. 6146 - 6151 (2012/09/07)

In this article we describe a new accessible methodology for the synthesis of isobenzofuran-1(3H)-ones. In this process we exploited an effective, economic, useful and environmentally benign K2CO3 catalyzed, solvent-free one-pot tandem aldol-lactonization reaction between active methylene compounds and methyl 2-carboxy benzaldehyde. A particularly simple work-up and purification procedure are additional advantages addressed to a general green chemistry approach to this important class of heterocyclic compounds.

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