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8-hydroxy-9,10-dioxo-1,4,4a,9,9a,10-hexahydroanthracen-1-yl acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

70063-65-9

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70063-65-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 70063-65-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,0,6 and 3 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 70063-65:
(7*7)+(6*0)+(5*0)+(4*6)+(3*3)+(2*6)+(1*5)=99
99 % 10 = 9
So 70063-65-9 is a valid CAS Registry Number.

70063-65-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (8-hydroxy-9,10-dioxo-1,4,4a,9a-tetrahydroanthracen-1-yl) acetate

1.2 Other means of identification

Product number -
Other names -

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:70063-65-9 SDS

70063-65-9Downstream Products

70063-65-9Relevant academic research and scientific papers

CHANGES OF STEREOSELECTIVITY AND RATE IN DIELS-ALDER REACTIONS BY HYDROPHOBIC SOLVENT EFFECTS AND BY BOVINE SERUM ALBUMIN

Colonna, Stefano,Manfredi, Amedea,Annunziata, Rita

, p. 3347 - 3350 (1988)

The use of water instead of benzene as the solvent can strongly influence the stereoselectivity and the rate of Diels-Alder reactions of 1,4-naphthoquinone derivatives with different dienes.Enantiomeric exess (e.e.) up to 38percent is reached in the presence of a catalytic amount of bovine serum albumin.

The 'Mikami'-Catalyst in Enantioselective Diels-Alder Reactions of Juglone-Based Dienophiles with Different 1-Oxygenated Dienes: An Investigation on the Substitution Pattern Dependent Regioselectivity

B?se, Dietrich,Frey, Wolfgang,Pietruszka, J?rg

, p. 2524 - 2532 (2015/12/26)

A mechanistic study investigating the substitution pattern depending regioselectivity of enantioselective BINOL-Ti-catalyzed- Diels-Alder reactions of juglone-based dienophiles with 1-oxygenated dienes is reported. The different influences of residues both on the diene as well as on the dienophiles are investigated giving a detailed picture of their role on the regioselectivity.

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