2999-40-8 Usage
Description
Phloroglucinol triacetate is a chemical compound derived from phloroglucinol, a polyphenol found in plants such as certain fruiting bodies and some species of oak. It is most commonly used as a pharmaceutical intermediate, particularly in the production of antispasmodic drugs. Phloroglucinol triacetate functions as a reducing agent and has the ability to protect against oxidative stress. Its versatile chemical reactivity and pharmacological properties make it an important and valuable compound in the field of medicinal chemistry and organic synthesis.
Uses
Used in Pharmaceutical Industry:
Phloroglucinol triacetate is used as a pharmaceutical intermediate for the production of antispasmodic drugs. It helps in the synthesis of these drugs, which are used to relieve muscle spasms and cramps.
Used in Organic Synthesis:
Phloroglucinol triacetate is used as a reducing agent in organic synthesis. Its ability to protect against oxidative stress makes it a valuable compound in the synthesis of various organic compounds.
Used in Fragrance Industry:
Phloroglucinol triacetate has potential applications in the synthesis of fragrances. Its unique chemical properties contribute to the creation of various scent profiles in the fragrance industry.
Used in Dye Industry:
Phloroglucinol triacetate is also used in the synthesis of dyes. Its versatile chemical reactivity allows for the development of a wide range of dyes with different color properties.
Check Digit Verification of cas no
The CAS Registry Mumber 2999-40-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,9 and 9 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2999-40:
(6*2)+(5*9)+(4*9)+(3*9)+(2*4)+(1*0)=128
128 % 10 = 8
So 2999-40-8 is a valid CAS Registry Number.
2999-40-8Relevant articles and documents
COMPOUNDS, PHARMACEUTICAL COMPOSITIONS AND USE THEREOF AS INHIBITORS OF RAN GTPASE
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Paragraph 0097; 00120, (2019/04/09)
Compounds of general formula IA, IB and IC outlined below, including pharmaceutically acceptable salts, solvates and hydrates thereof. Such compounds and pharmaceutical compositions comprising them may be used in medical conditions involving Ran GTPase.
Protection of COOH and OH groups in acid, base and salt free reactions
Zhu, Xiaotao,Qian, Bo,Wei, Rongbiao,Huang, Jian-Dong,Bao, Hongli
supporting information, p. 1444 - 1447 (2018/04/12)
We report an iron-catalyzed general functional group protection method with inexpensive reagents. This environmentally benign process does not use acids or bases, and does not produce waste products. Further purification beyond filtration and evaporation is, in most cases, unnecessary. Free COOH and OH groups can be protected in a one-pot reaction.
Synthesis and antibacterial activity of new symmetric polyoxygenated dibenzofurans
Oramas-Royo, Sandra,Pantoja, Kriss Dayana,Amesty, ángel,Romero, Carmen,Lorenzo-Castrillejo, Isabel,Machín, Félix,Estévez-Braun, Ana
, p. 178 - 187 (2017/10/16)
A series of symmetric polyoxygenated dibenzofurans with 2-methylbutyril moieties at C-4 and C-6 were obtained from commercial phloroglucinol through a sequence of reactions that include monoacylation, iodination, Suzuki-Miyaura coupling, oxidative dimeriz
