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14107-97-2

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14107-97-2 Usage

Description

2,4,6-TRIMETHOXYTOLUENE, also known as TMT, is a chemical compound characterized by the molecular formula C9H12O3. It is a colorless to pale yellow liquid with a distinctive floral scent. TMT is primarily utilized as an intermediate in the synthesis of fragrances and perfumes, contributing to the creation of various aromatic compounds. Additionally, it serves as a solvent in the production of resins, adhesives, and coatings, highlighting its versatility in industrial applications. Despite its low acute toxicity, prolonged exposure to high concentrations of TMT may result in skin, eye, and respiratory irritation, necessitating proper handling and safety measures.

Uses

Used in the Fragrance and Perfumery Industry:
2,4,6-TRIMETHOXYTOLUENE is used as an intermediate in the synthesis of fragrances and perfumes for its ability to contribute to the creation of a wide range of aromatic compounds. Its floral scent adds depth and complexity to various fragrance formulations, enhancing the overall sensory experience.
Used in the Production of Resins, Adhesives, and Coatings:
2,4,6-TRIMETHOXYTOLUENE is used as a solvent in the manufacturing process of resins, adhesives, and coatings. Its solvent properties facilitate the blending and application of these materials, ensuring optimal performance and adherence to various surfaces. The use of TMT in these applications underscores its importance in the production of a diverse array of industrial products.

Check Digit Verification of cas no

The CAS Registry Mumber 14107-97-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,1,0 and 7 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 14107-97:
(7*1)+(6*4)+(5*1)+(4*0)+(3*7)+(2*9)+(1*7)=82
82 % 10 = 2
So 14107-97-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H14O3/c1-7-9(12-3)5-8(11-2)6-10(7)13-4/h5-6H,1-4H3

14107-97-2 Well-known Company Product Price

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  • Alfa Aesar

  • (L02155)  2,4,6-Trimethoxytoluene, 97%   

  • 14107-97-2

  • 5g

  • 951.0CNY

  • Detail
  • Alfa Aesar

  • (L02155)  2,4,6-Trimethoxytoluene, 97%   

  • 14107-97-2

  • 25g

  • 3641.0CNY

  • Detail

14107-97-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3,5-trimethoxy-2-methylbenzene

1.2 Other means of identification

Product number -
Other names Benzene,1,3,5-trimethoxy-2-methyl

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:14107-97-2 SDS

14107-97-2Relevant articles and documents

Efficient synthesis of rottlerin and its two subunits

Li, Yangfeng,Yu, Biao,Wang, Renxiao

, p. 1856 - 1859 (2016)

Rottlerin, a natural product isolated from Mallotus philippensis, is associated with a range of biological activities. Its chemical structure is featured by two different substituted phloroglucinol units linked by a methylene group. In this study, we accomplished a total synthesis of rottlerin using phenol-aldehyde condensation as the key reaction. By our method, gram-scale preparation of the two structural subunits was achieved, and rottlerin was obtained in a longest eight linear step with 20% overall yield. Our study provides a practical solution for obtaining the sample of rottlerin in an efficient way.

Phloroglucinol derivatives as anti-tumor agents: synthesis, biological activity evaluation and molecular docking studies

Zhang, Fuli,Lai, Qingfu,Lai, Weihong,Li, Ming,Jin, Xiaobao,Ye, Lianbao

, p. 165 - 176 (2021/12/02)

Phloroglucinol compounds isolated from Dryopteris fragrans (L.) Schott showed a variety of biological activities, such as anticancer and anti-inflammatory. In this study, we have made a number of modifications around the scaffold of phloroglucinol and synthesized phloroglucinol derivatives A1–A9, B1–B9, and C1–C3. We synthesized these compounds and investigated their effect on four human cancer cell lines (A-549, MCF-7, Hela, HepG2 cell lines) via MTT assay in vitro. The results revealed that all compounds exhibited certain antiproliferative activities on cancer cell lines and excellent inhibitory effects on MCF-7, in which compound C2 was the best with the IC50 value of 18.49 μM, exceeding that of 5-fluorouracil. Moreover, the cell apoptosis test showed that compound C2 induced apoptosis in a concentration-dependent manner. Furthermore, the results of molecular docking analysis explained the probable interaction between the active compounds and active sites of target protein 4I22 and 1OG5. [Figure not available: see fulltext.]

Dryopteris fragrans phloroglucinol compound flavaspidic acid BB and antibacterial application thereof

-

, (2018/05/24)

The invention relates to the technical field of medicine and discloses an antibacterial application of a Dryopteris fragrans phloroglucinol compound flavaspidic acid BB. The invention provides the flavaspidic acid BB obtained by the chemical synthesis method. The flavaspidic acid BB has good antibacterial effects, effectively fills in the application deficiency of the antibacterial natural compound and provides an effective antibacterial solution for drug-resistant bacteria. The experimental results show that the compound has a strong antibacterial effect and good curative effects especially on drug-resistant bacteria.

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