60088-54-2 Usage
Description
TEREPHTHALIC-D4 ACID, also known as isotope labeled Terephthalic acid, is a benzenepolycarboxylic acid that exhibits potential anti-hemorrhagic properties. It is a compound with a unique molecular structure, which allows it to be used in various applications across different industries.
Uses
Used in Pharmaceutical Industry:
TEREPHTHALIC-D4 ACID is used as a pharmaceutical agent for its potential anti-hemorrhagic properties. It can be utilized in the development of treatments and therapies for conditions related to excessive bleeding or hemorrhage.
Used in Chemical Research:
TEREPHTHALIC-D4 ACID, being an isotope labeled compound, is used as a research tool in chemical studies. It aids in understanding the behavior and properties of similar compounds, as well as in tracking metabolic pathways and reactions in various chemical processes.
Used in Material Science:
In the field of material science, TEREPHTHALIC-D4 ACID can be employed as a component in the synthesis of advanced materials. Its unique properties may contribute to the development of new materials with specific characteristics, such as improved strength, durability, or other desirable traits.
Used in Environmental Studies:
TEREPHTHALIC-D4 ACID can also be utilized in environmental studies to monitor and track the presence of pollutants or contaminants in various ecosystems. Its isotope labeled nature allows for more accurate detection and analysis of these substances, contributing to a better understanding of their impact on the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 60088-54-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,0,8 and 8 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 60088-54:
(7*6)+(6*0)+(5*0)+(4*8)+(3*8)+(2*5)+(1*4)=112
112 % 10 = 2
So 60088-54-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H6O4/c9-7(10)5-1-2-6(4-3-5)8(11)12/h1-4H,(H,9,10)(H,11,12)/i1D,2D,3D,4D
60088-54-2Relevant articles and documents
SELECTIVE MONO- OR DIMETALATION OF ARENES BY MEANS OF SUPERBASIC REAGENTS
Schlosser, Manfred,Choi, Jung Hoon,Takagishi, Sadahito
, p. 5633 - 5648 (2007/10/02)
If employed in tetrahydrofuran, stoichiometric amounts of butyllithium and potassium tert-butoxide react with benzene under clean monometalation.In hexane suspension, however, considerable amounts of meta- and para-disubstituted by-products are obtained (approx. 10percent).They become preponderant if a three-fold excess of the metalating agent is used.Naphthalene leads under the same conditions to a mixture of two mono- and ten di-substituted derivatives. - Alkyl groups, as present in tert-butylbenzene, retard the metalation at both m- and p-positions, while trialkylsilyl groups deactivate only m-position.In either case exclusive monosubstitution occurs. - Perdeuterobenzene undergoes metalation and subsequent electrophilic mono- or disubstitution to afford isotope labeled compounds with moderate, though synthetically attractive yields.The kinetic isotope effects and product ratios can be taken as evidence for aggregate formation at the level of both the superbasic metalating reagent and the organometallic intermediates.
