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Isobenzofuran, 1,3-dihydro-4,5,6,7-tetraphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

61051-01-2

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61051-01-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61051-01-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,0,5 and 1 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 61051-01:
(7*6)+(6*1)+(5*0)+(4*5)+(3*1)+(2*0)+(1*1)=72
72 % 10 = 2
So 61051-01-2 is a valid CAS Registry Number.

61051-01-2SDS

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 4,5,6,7-tetraphenyl-1,3-dihydro-2-benzofuran

1.2 Other means of identification

Product number -
Other names Isobenzofuran,1,3-dihydro-4,5,6,7-tetraphenyl

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:61051-01-2 SDS

61051-01-2Downstream Products

61051-01-2Relevant academic research and scientific papers

Effect of substituents at 1,4-positions of polycyclic aromatic compounds and preparation of 2,3-difunctionalized pentacenes and naphthacenes

Li, Shi,Zhou, Lishan,Song, Zhiyi,Bao, Fengyu,Kanno, Ken-ichiro,Takahashi, Tamotsu

, p. 519 - 536 (2007)

Effects of substituents at 1,4-positions of polycyclic aromatic compounds were investigated in the case of reduction of 2,3-bis(alkoxycarbonyl)arenes with the LiAlH4/AlCI3 system. 2,3-Bis(alkoxycarbonyl)dihydronaphthacenes and dihydropentacenes 1 were treated with a mixture of LiAlH4 and AlCl3. The products were dependent on the substituents at 1,4-positions. Similar type of influence of the substituents at 1,4-positions was observed in the oxidation of diols 2 to dialdehydes 4. Without substituents at 1,4-positions, dialdehydes 4 were conveniently obtained. However, with substituents at 1,4-positions, dialdehydes 4 were not obtained. Instead,1,3-dihydroisobenzofuran-l,3-diol or 1,3-dihydroisobenzofuran-l-ol derivatives 5, 6 were obtained in good yields. Preparation of pentacene imides and pentacene carboxylic acid anhydride was also reported.

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