29652-81-1 Usage
Description
1-(3,4,5-Trimethoxyphenyl)Propan-1-Ol, with the molecular formula C12H18O4, is a colorless, viscous liquid characterized by a sweet, floral odor. This chemical compound is recognized for its synthetic applications in various industries, including fragrance and flavor production, pharmaceuticals, and agrochemicals. It serves as an intermediate in organic synthesis, contributing to the creation of scents and flavors that mimic natural substances. Despite its utility, it is crucial to handle 1-(3,4,5-Trimethoxyphenyl)Propan-1-Ol with caution and adhere to safety protocols due to its potential hazards.
Uses
Used in Fragrance and Flavor Industry:
1-(3,4,5-Trimethoxyphenyl)Propan-1-Ol is used as a synthetic ingredient for creating scents and flavors that resemble natural substances. Its sweet, floral odor makes it a valuable addition to the fragrance and flavor industry, enhancing the sensory experience of various products.
Used in Pharmaceutical Production:
In the pharmaceutical sector, 1-(3,4,5-Trimethoxyphenyl)Propan-1-Ol is utilized in the development and manufacturing of various medicinal compounds. Its chemical properties contribute to the formulation of drugs, playing a significant role in the pharmaceutical industry.
Used in Agrochemicals:
1-(3,4,5-Trimethoxyphenyl)Propan-1-Ol also finds application in the agrochemical industry, where it is employed in the production of chemical compounds used in agriculture. Its role in this sector is vital for enhancing crop protection and productivity.
Used as an Intermediate in Organic Synthesis:
Furthermore, 1-(3,4,5-Trimethoxyphenyl)Propan-1-Ol serves as an intermediate in organic synthesis, facilitating the creation of a wide range of chemical compounds. Its versatility in this capacity makes it an essential component in various chemical reactions and processes.
Check Digit Verification of cas no
The CAS Registry Mumber 29652-81-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,6,5 and 2 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 29652-81:
(7*2)+(6*9)+(5*6)+(4*5)+(3*2)+(2*8)+(1*1)=141
141 % 10 = 1
So 29652-81-1 is a valid CAS Registry Number.
29652-81-1Relevant articles and documents
Alpha,beta-unsaturated ketone derivatives, preparation method of derivatives and application of derivatives as medicines
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Paragraph 0073-0076, (2019/12/15)
The invention relates to the technical field of medicine, and proposes alpha,beta-unsaturated ketone derivatives and a preparation method thereof. The derivatives have a structural general formula represented by a formula I shown in the specification, whe
Combretastatin-like chalcones as inhibitors of microtubule polymerization. Part 1: Synthesis and biological evaluation of antivascular activity
Ducki, Sylvie,Rennison, David,Woo, Meiko,Kendall, Alexander,Chabert, Jeremie Fournier Dit,McGown, Alan T.,Lawrence, Nicholas J.
experimental part, p. 7698 - 7710 (2010/03/24)
The α-methyl chalcone SD400 is a potent inhibitor of tubulin assembly and possesses potent anticancer activity. Various chalcone analogues were synthesized and evaluated for their cell growth inhibitory properties against the K562 human chronic myelogenous leukemia cell line (SD400, IC50 0.21 nM; combretastatin A4 CA4, IC50 2.0 nM). Cell cycle analysis by flow cytometry indicated that these agents are antimitotic (SD400, 83% of the cells are in G2/M phase; CA4 90%). They inhibit tubulin assembly at low concentration (SD400, IC50 0.46 μM; CA4, 0.10 μM) and compete with [3H]colchicine for binding to tubulin (8% [3H]colchicine remained bound to tubulin after competition with SD400 or CA4). Upon treatment with SD400, remarkable cell shape changes were elicited in HUVEC cells, consistent with vasculature damaging activity.
Unexpected formation of aryl dialkyl carbinol as a side product from the reaction of methoxyarylaldehydes with Grignard reagents
Sharma, Anuj,Joshi, Bhupendra P.,Singh, Narendra P.,Sinha, Arun K.
, p. 847 - 851 (2007/10/03)
In the attempted formation of secondary aryl alkyl carbinols from the reaction of methoxyarylaldehydes with Grignard reagents, aryl dialkyl carbinols were formed as unexpected side products. A mechanism for their formation is proposed.
