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13427-80-0

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13427-80-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13427-80-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,4,2 and 7 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 13427-80:
(7*1)+(6*3)+(5*4)+(4*2)+(3*7)+(2*8)+(1*0)=90
90 % 10 = 0
So 13427-80-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H6O4.2K/c9-7(10)5-1-2-6(4-3-5)8(11)12;;/h1-4H,(H,9,10)(H,11,12);;/q;2*+1/p-2

13427-80-0SDS

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 terephthalic acid dipotassium salt

1.2 Other means of identification

Product number -
Other names potassium terephthalate dibasic

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:13427-80-0 SDS

13427-80-0Relevant articles and documents

Surface modified EuxLa1-xF3 nanoparticles as luminescent biomarkers: Still plenty of room at the bottom

Khudoleeva, Vladislava Yu.,Utochnikova, Valentina V.,Kalyakina, Alena S.,Deygen, Irina M.,Shiryaev, Andrey A.,Marciniak, ?ukasz,Lebedev, Vasiliy A.,Roslyakov, Ilya V.,Garshev, Alexey V.,Lepnev, Leonid S.,Schepers, Ute,Br?se, Stefan,Kuzmina, Natalia P.

, p. 348 - 355 (2017)

Investigation of the formation and luminescent properties of surface modified bimetallic lanthanide fluorides and their use in bioimaging is described. We have shown that the solvent during the wet synthesis of EuF3 nanoparticles affects the na

GREEN, COPPER-CATALYZED DISPROPORTIONATION OF AROMATIC AND HETEROAROMATIC CARBOXYLATES TO DICARBOXYLATES

-

Paragraph 0123-0125, (2020/06/08)

The present application relates to a process for preparation of a compound of Formula (I) and Formula (IV): wherein is as described herein; and wherein and R are as described herein.

An improved and practical synthesis of tranexamic acid

Li, Zhenhua,Fang, Li,Wang, Jian,Dong, Liuhong,Guo, Yanna,Xie, Yuanyuan

, p. 444 - 448 (2015/03/30)

Tranexamic acid 1, a synthetic antifibrinolytic drug with the treatment being considered highly cost-effective in many countries, has been included in the WHO list of essential medicines. In this paper, we designed the synthesis of 1 via a novel seven-step route from the readily available starting material dimethyl terephthalate, performing with 99.6% purity in 59.2% overall yield. During the process, we successfully developed a direct and efficient method for the preparation of key intermediate methyl 4-(acetamidomethyl)benzoate by one-pot hydrogenation and acylation in acetic anhydride using Ni/Al2O3 as a catalyst. More importantly, it should be a straightforward and practical way to circumvent the usage of toxic reagents (CrO3, Cl2), solvent (CCl4), and expensive catalyst (PtO2), etc., that plagued the previous methodologies.

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