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1(2H)-Naphthalenone, 3,4-dihydro-2-hydroxy-2-(1-methylethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

78507-00-3

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78507-00-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 78507-00-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,5,0 and 7 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 78507-00:
(7*7)+(6*8)+(5*5)+(4*0)+(3*7)+(2*0)+(1*0)=143
143 % 10 = 3
So 78507-00-3 is a valid CAS Registry Number.

78507-00-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-hydroxy-2-isopropyl-3,4-dihydronaphthalen-1(2H)-one

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:78507-00-3 SDS

78507-00-3Downstream Products

78507-00-3Relevant academic research and scientific papers

STUDIES ON THE TERPENOIDS AND RELATED ALICYCLIC COMPOUNDS XXII STEREOCHEMICAL STUDY ON THE ANGULAR HYDROXYLATION OF POLYCYCLIC KETONES USING BENZENESELENINIC ANHYDRIDE

Yamakawa, Koji,Satoh, Tsuyoshi,Ohba, Nobuyuki,Sakaguchi, Reiji,Takita, Satoshi,Tamura, Nobuhiko

, p. 473 - 480 (1981)

Introduction of an OH group to the tertiary carbon of simple ketones (1, 2 and 6), furanoeremophilane-type ketones (12-19), and tricyclic ketones (20-22) by the use of benzeneseleninic anhydride is described. 10β-Hydroxy compounds were obtained in the case of 12-14, and 20-22. 10α-Hydroxy compounds were obtained in the case of 15 and 16.In the hydroxylation reaction of polycyclic ketones using benzeneseleninic anhydride, the results suggest that the thermodynamically more stable product was usually produced as the major product.

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