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97971-75-0

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97971-75-0 Usage

Preparation

reparation from lin-parabenzotetraphenyl-–difurfuran by oxidation with chromium trioxide in refluxing acetic anhydride for >1 h, followed by saponification of the 2,5-dibenzoylhydroquinone dibenzo-ate so formed with potassium hydroxide in ethanol in a water bath for 30 min (43%).

Check Digit Verification of cas no

The CAS Registry Mumber 97971-75-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,9,7 and 1 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 97971-75:
(7*9)+(6*7)+(5*9)+(4*7)+(3*1)+(2*7)+(1*5)=200
200 % 10 = 0
So 97971-75-0 is a valid CAS Registry Number.

97971-75-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-benzoyl-2,5-dihydroxyphenyl)-phenylmethanone

1.2 Other means of identification

Product number -
Other names 2,5-dibenzoyl-1,4-dihydroxybenzene

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:97971-75-0 SDS

97971-75-0Relevant articles and documents

Facile synthesis of regio-isomeric naphthofurans and benzodifurans

Park, Kwanghee Koh,Jeong, Jinsuk

, p. 545 - 553 (2007/10/03)

Naphtho[1,2-b]furans 1a-f, naphtho[2,1-b]furans 2a-f, benzo[1,2-b:5,4- b′]difurans 3a-b, benzo[1,2-b:4,5-b′]difurans 4a-b, and benzo[1,2-b:4,3-b′]difurans 5a-b were synthesized by base-catalyzed cyclization reaction of the corresponding o-alkoxybenzoylarene derivatives. The o-alkoxybenzoylarenes were obtained from the etherification reaction of the o-hydroxybenzoylarenes, which were prepared either by the reaction of methoxyarenes with benzoyl chloride in the presence of aluminum chloride or by photo-Fries rearrangement of aryl benzoates. Graphical Abstract.

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