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34883-80-2

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34883-80-2 Usage

Chemical Family

Isobenzofuranones

Cyclic Organic Molecule

Yes

Contains

Furan ring

Additional Groups

Naphthalene group and a methylene group

Usage

Organic chemistry

Potential Applications

Industrial and research processes

Unique Structure

Yes

Potential Uses

Pharmaceuticals or materials science

Implications

Wide range of scientific and industrial purposes

Check Digit Verification of cas no

The CAS Registry Mumber 34883-80-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,8,8 and 3 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 34883-80:
(7*3)+(6*4)+(5*8)+(4*8)+(3*3)+(2*8)+(1*0)=142
142 % 10 = 2
So 34883-80-2 is a valid CAS Registry Number.

34883-80-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-naphthalen-1-ylmethylene-3H-isobenzofuran-1-one

1.2 Other means of identification

Product number -
Other names ([1]-Naphthyl-methylen)-phthalid

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:34883-80-2 SDS

34883-80-2Relevant articles and documents

Catalytic enantioselective synthesis of chiral phthalides by efficient reductive cyclization of 2-acylarylcarboxylates under aqueous transfer hydrogenation conditions

Zhang, Bo,Xu, Ming-Hua,Lin, Guo-Qiang

supporting information; experimental part, p. 4712 - 4715 (2009/12/08)

A new diamine ligand for asymmetric transfer hydrogenation (ATH) was discovered. The reductive cyclization of 2-acylarylcarboxylates was found to proceed highly stereoselective by the new Ru complex-catalyzed ATH and subsequent In situ lactonization under aqueous conditions. It enables efficient access to a wide variety of 3-substituted phthalides In enantiomerically pure form.

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