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1,4-Naphthalenedione, 2-methyl-3-(1-methylethyl)-, also known as 2-Methyl-3-isopropylnaphthalene-1,4-dione, is an organic compound with the chemical formula C14H14O2. It is a derivative of naphthalene, a polycyclic aromatic hydrocarbon, and features a diketone functional group at the 1,4-positions, a methyl group at the 2-position, and an isopropyl group at the 3-position. 1,4-Naphthalenedione, 2-methyl-3-(1-methylethyl)- is primarily used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. Due to its complex structure and potential applications, it is an important molecule in the field of organic chemistry and chemical engineering.

34711-52-9

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34711-52-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 34711-52-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,7,1 and 1 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 34711-52:
(7*3)+(6*4)+(5*7)+(4*1)+(3*1)+(2*5)+(1*2)=99
99 % 10 = 9
So 34711-52-9 is a valid CAS Registry Number.

34711-52-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methyl-3-propan-2-ylnaphthalene-1,4-dione

1.2 Other means of identification

Product number -
Other names 2-isopropyl-3-methyl-1,4-naphthoquinone

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:34711-52-9 SDS

34711-52-9Downstream Products

34711-52-9Relevant academic research and scientific papers

HOMOLYTIC ALKYLATION OF NAPHTHOQUINONE AND METHYL-NAPHTHOQUINONE. ENTHALPIC, STERIC AND POLAR EFFECTS.

Coppa, F.,Fontana, F.,Minisci, F.,Barbosa, M. C. Nogueira,Vismara, E.

, p. 7343 - 7352 (1991)

The homolytic methylation of naphthoquinone to obtain menadione has been investigated by three sources of methyl radical: t-BuOOH, DMSO and H2O2, acetone and H2O2.Moreover the homolytic alkylation of naphthoquinone and 2-methylnaphthoquinone has been investigated by using alkyl iodides as sources of alkyl radicals.

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