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2-tert-butyl-3-methylnaphthalene-1,4-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

75909-62-5

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75909-62-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 75909-62-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,9,0 and 9 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 75909-62:
(7*7)+(6*5)+(5*9)+(4*0)+(3*9)+(2*6)+(1*2)=165
165 % 10 = 5
So 75909-62-5 is a valid CAS Registry Number.

75909-62-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-tert-butyl-3-methylnaphthalene-1,4-dione

1.2 Other means of identification

Product number -
Other names 2-tert-butyl-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:75909-62-5 SDS

75909-62-5Downstream Products

75909-62-5Relevant academic research and scientific papers

Visible Light-Induced Decarboxylative Alkylation of Heterocyclic Aromatics with Carboxylic Acids via Anthocyanin as a Photocatalyst

Guo, Rui,Zuo, Minghui,Tian, Qinye,Hou, Chuanfu,Sun, Shouneng,Guo, Weihao,Wu, Hongfeng,Chu, Wenyi,Sun, Zhizhong

, p. 1976 - 1981 (2020/06/01)

A visible light-induced decarboxylative alkylation of heterocyclic aromatics with aliphatic carboxylic acids was developed by using anthocyanins as a photocatalyst under mild conditions. A series of alkylated heterocyclic compounds were obtained in modera

Solvent, chelation and concentration effects on the benzannulation reaction of chromium carbene complexes and acetylenes

Chan, Kin Shing,Peterson, Glen A.,Brandvold, Timothy A.,Faron, Katherine L.,Challener, Cynthia, A.,et al.

, p. 9 - 56 (2007/10/02)

The reactions of a number of chromium carbene complexes (CO)5Cr=C(OMe)R (R = Ph, o-OMePh, p-OMePh, o-O-tBuPh, 1-C6H9, 1-C5H7O) were examined with a variety of acetylenes (R'CCR2, R1, R2 = H, Me, Et, n-Pr, Ph, SiMe3) in sol

THE DEVELOPMENT OF AN ORGANOTRANSITION METAL SYNTHESIS OF QUINONES

Liebeskind, Lenny S.,Baysdon, Sherol L.,South, Michael S.,Iyer, Suresh,Leeds, James P.

, p. 5839 - 5853 (2007/10/02)

A new and very general synthesis of quinones is described from conception to the current state of maturity.The chemistry relies on a convergent joining of a transition metal complex and an alkyne to provide benzoquinones (from maleoylmetal complexes) and naphthoquinones (from phthaloylmatal complexes).Significant aspects of this chemistry are its generality (terminal, internal, electron rich, and electron deficient alkynes react), its mildness (reactions can be run between room temperature and 80 deg C) and its functional group compabtibility (aldehydes, ketones, esters, nitriles, olefins, halides acetals, ketals, etc. survive).

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