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METHYL 2-PHENOXYNICOTINATE is a chemical compound that belongs to the group of nicotinate esters. It is primarily used as a pharmaceutical intermediate and is also a common ingredient in a variety of cosmetic and personal care products. It exhibits both anti-inflammatory and analgesic properties, making it useful in the formulation of topical pain relief products. Additionally, it has been studied for its potential use in the treatment of various skin conditions and as a hair growth promoter. METHYL 2-PHENOXYNICOTINATE is also known for its pleasant odor, making it a popular choice for fragrance applications in perfumes and other scented products.

36701-88-9

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36701-88-9 Usage

Uses

Used in Pharmaceutical Industry:
METHYL 2-PHENOXYNICOTINATE is used as a pharmaceutical intermediate for the synthesis of various drugs.
Used in Cosmetic and Personal Care Industry:
METHYL 2-PHENOXYNICOTINATE is used as an ingredient in a variety of cosmetic and personal care products due to its anti-inflammatory and analgesic properties.
Used in Topical Pain Relief Products:
METHYL 2-PHENOXYNICOTINATE is used as an active ingredient in the formulation of topical pain relief products, providing relief from pain and inflammation.
Used in Skin Care Products:
METHYL 2-PHENOXYNICOTINATE has been studied for its potential use in the treatment of various skin conditions, making it a valuable ingredient in skin care products.
Used in Hair Care Products:
METHYL 2-PHENOXYNICOTINATE is used as a hair growth promoter in hair care products, contributing to healthier and thicker hair.
Used in Fragrance Industry:
METHYL 2-PHENOXYNICOTINATE is used in perfumes and other scented products due to its pleasant odor, enhancing the overall fragrance experience.

Check Digit Verification of cas no

The CAS Registry Mumber 36701-88-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,7,0 and 1 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 36701-88:
(7*3)+(6*6)+(5*7)+(4*0)+(3*1)+(2*8)+(1*8)=119
119 % 10 = 9
So 36701-88-9 is a valid CAS Registry Number.
InChI:InChI=1/C13H11NO3/c1-16-13(15)11-8-5-9-14-12(11)17-10-6-3-2-4-7-10/h2-9H,1H3

36701-88-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 2-phenoxypyridine-3-carboxylate

1.2 Other means of identification

Product number -
Other names Methyl 2-phenoxy-3-pyridinecarboxylate

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:36701-88-9 SDS

36701-88-9Downstream Products

36701-88-9Relevant academic research and scientific papers

PYRIDAZINONES AND METHODS OF USE THEREOF

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Page/Page column 132, (2019/04/11)

Disclosed are compounds according to Formula (A), and related tautomers and pharmaceutical compositions. Also disclosed are therapeutic methods, e.g., of treating kidney diseases, using the compounds of Formula (A).

Design, Synthesis, and Structure-Activity Relationship of New Pyrimidinamine Derivatives Containing an Aryloxy Pyridine Moiety

Guan, Aiying,Liu, Changling,Chen, Wei,Yang, Fan,Xie, Yong,Zhang, Jinbo,Li, Zhinian,Wang, Mingan

, p. 1272 - 1280 (2017/02/23)

The pyrimidinamine diflumetorim is an ideal template for the discovery of agrochemical lead compounds due to its unique mode of action, novel chemical structure, and lack of reported resistance. To develop a new pyrimidinamine fungicide effective against cucumber downy mildew (CDM), a series of new pyrimidinamine derivatives containing an aryloxy pyridine moiety were designed and synthesized by employing the recently reported intermediate derivatization method (IDM). The structures of all compounds were identified by 1H NMR, elemental analyses, HRMS, and X-ray diffraction. Bioassays demonstrated that some of the title compounds exhibited excellent fungicidal activities against CDM. Compound 9 gave the best activity (EC50 = 0.19 mg/L), which is significantly better than the commercial fungicides diflumetorim, flumorph, and cyazofamid. The relationship between structure and fungicidal activity of the synthesized pyrimidinamines was explored. The study showed that compound 9 is a promising fungicide candidate for further development.

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