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64139-21-5

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64139-21-5 Usage

General Description

Diethyl 4-hydroxyphthalate is a chemical compound that belongs to the family of phthalate esters. It is often used as a plasticizer in the manufacturing of various products such as adhesives, coatings, and films. It is also utilized in the production of synthetic resins, and as an intermediate in the synthesis of various organic compounds. This chemical is considered to have low acute toxicity, although it may present some health risks if handled improperly. There is ongoing research to explore its potential impacts on human health and the environment, particularly in relation to its use in consumer products.

Check Digit Verification of cas no

The CAS Registry Mumber 64139-21-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,1,3 and 9 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 64139-21:
(7*6)+(6*4)+(5*1)+(4*3)+(3*9)+(2*2)+(1*1)=115
115 % 10 = 5
So 64139-21-5 is a valid CAS Registry Number.
InChI:InChI=1/C12H14O5/c1-3-16-11(14)9-6-5-8(13)7-10(9)12(15)17-4-2/h5-7,13H,3-4H2,1-2H3

64139-21-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name diethyl 4-hydroxybenzene-1,2-dicarboxylate

1.2 Other means of identification

Product number -
Other names Diethyl-4-hydroxyphthalat

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:64139-21-5 SDS

64139-21-5Relevant articles and documents

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Miller

, p. 1092 (1878)

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Conversion of Simple Cyclohexanones into Catechols

Liang, Yu-Feng,Li, Xinyao,Wang, Xiaoyang,Zou, Miancheng,Tang, Conghui,Liang, Yujie,Song, Song,Jiao, Ning

, p. 12271 - 12277 (2016/09/28)

A novel I2-catalyzed direct conversion of cyclohexanones to substituted catechols under mild and simple conditions has been described. This novel transformation is remarkable with the multiple oxygenation and dehydrogenative aromatization processes enabled just by using DMSO as the solvent, oxidant, and oxygen source. This metal-free and simple system demonstrates a versatile protocol for the synthesis of highly valuable substituted catechols and therefore streamlines the synthesis and modification of biologically important molecules for drug discovery.

RHODAMINE COMPOUNDS AND THEIR USE AS FLUORESCENT LABELS

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Page/Page column 52-53, (2014/09/29)

The present invention relates to new rhodamine compounds and their use as fluorescent labels. The compounds may be used as fluorescent labels for nucleotides in nucleic acid sequencing applications.

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