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1-Naphthalenecarboxylic acid, 2,3-dibenzoyl-1,2-dihydro-4-hydroxy- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

88036-08-2

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88036-08-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88036-08-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,0,3 and 6 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 88036-08:
(7*8)+(6*8)+(5*0)+(4*3)+(3*6)+(2*0)+(1*8)=142
142 % 10 = 2
So 88036-08-2 is a valid CAS Registry Number.

88036-08-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-benzoyl-3-[hydroxy(phenyl)methylidene]-4-oxo-1,2-dihydronaphthalene-1-carboxylic acid

1.2 Other means of identification

Product number -
Other names 1-Naphthalenecarboxylic acid,2,3-dibenzoyl-1,2-dihydro-4-hydroxy

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:88036-08-2 SDS

88036-08-2Downstream Products

88036-08-2Relevant academic research and scientific papers

Strong Base Induced Cycloaddition of Homophthalic Anhydrides Leading to peri-Hydroxy Polycyclic Compounds

Tamura, Yasumitsu,Sasho, Manabu,Nakagawa, Kiyomi,Tsugoshi, Teruhisha,Kita, Yasuyuki

, p. 473 - 478 (1984)

A new and exceptionally facile cycloaddition of the alkaline metal salt of homophthalic anhydrides (1a,b) is described.The anions of the anhydrides 1a,b undergo cycloadditions with various dienophiles (5-14) to give the corresponding peri-hydroxy polycyclic compounds (15-26) in good yields under extremely mild conditions, whereas thermal cycloaddition of 1a,b requires high temperatures.

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