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1(3H)-Isobenzofuranone, 6-(dimethylamino)-3-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

57489-62-0

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57489-62-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 57489-62-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,4,8 and 9 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 57489-62:
(7*5)+(6*7)+(5*4)+(4*8)+(3*9)+(2*6)+(1*2)=170
170 % 10 = 0
So 57489-62-0 is a valid CAS Registry Number.

57489-62-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-(dimethylamino)-3-phenyl-3H-2-benzofuran-1-one

1.2 Other means of identification

Product number -
Other names 3-phenyl-6-dimethylaminophthalide

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:57489-62-0 SDS

57489-62-0Downstream Products

57489-62-0Relevant academic research and scientific papers

Directed ortho metalation of n,n-diethyl benzamides. Methodology and regiospecific synthesis of useful contiguously tri- and tetra-substituted oxygenated aromatics, phthalides and phthalic anhydrides

De Silva,Reed,Billedeau,Wang,Norris,Snieckus

, p. 4863 - 4878 (2007/10/02)

Full experimental details for the directed ortho metalation approch to a variety of simple ortho-substituted N,N-diethyl benzamides (Table 1) and contiguously 1,2,3- and 1,2,3,4-substituted benzamides (Tables 2) are given. The efficient conversion of these benzamides (6, 10, 12, 13, 18, 19) into phthalides (9a-b, 16b-c, 17) and phthalic anhydrides (8,16a), compounds previously available by demanding, classical methods, is detailed. A short synthesis of iso-ochracinic acid (27) is described.

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