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2,5,8-Trimethyl-1-naphthol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

33583-02-7

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33583-02-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 33583-02-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,5,8 and 3 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 33583-02:
(7*3)+(6*3)+(5*5)+(4*8)+(3*3)+(2*0)+(1*2)=107
107 % 10 = 7
So 33583-02-7 is a valid CAS Registry Number.
InChI:InChI=1/C13H14O/c1-8-4-5-9(2)12-11(8)7-6-10(3)13(12)14/h4-7,14H,1-3H3

33583-02-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,5,8-trimethylnaphthalen-1-ol

1.2 Other means of identification

Product number -
Other names 2,5,8-TRIMETHYL-1-NAPHTHOL

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:33583-02-7 SDS

33583-02-7Downstream Products

33583-02-7Relevant academic research and scientific papers

Sequential and regioselective Friedel-Crafts reactions of gem-dihalocyclopropanecarbonyl chlorides with benzenes for the synthesis of 4-aryl-1-naphthol derivatives

Nishii, Yoshinori,Tanabe, Yoo

, p. 8803 - 8806 (1995)

Two types of novel, sequential and regioselective Friedel-Crafts reactions of gem-dihalocyclopropanecarbonyl chlorides with benzenes proceeded in a one-pot manner; E-3-aryl-2,2-dihalo-cyclopropanecarbonyl chlorides reacted with substituted benzenes to afford 4-aryl-3-halo-1-naphthols, while 2,2-dichlorocyclopropanecarbonyl chlorides were transformed into 4-aryl-1-naphthols in benzene or p-xylene. Both annulations involved alternative and highly regioselective cyclopropane ring-openings.

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