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Methyl 4-[3-(dimethylamino)propoxy]benzoate is a chemical compound classified as an ester. It is recognized for its ability to absorb and block ultraviolet (UV) radiation from the sun, making it a valuable ingredient in personal care products. Additionally, it contributes to skin conditioning properties, which enhances its utility in cosmetic and skincare formulations. Its versatility extends to the fragrance industry, where it is used in perfumes and other scented products. However, it is important to exercise caution with its use due to potential irritation or sensitization in some individuals.

190660-97-0

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190660-97-0 Usage

Uses

Used in Personal Care Industry:
Methyl 4-[3-(dimethylamino)propoxy]benzoate is used as an active ingredient in sunscreens, lotions, and moisturizers for its UV radiation absorption and blocking capabilities, providing protection to the skin from harmful sun exposure.
Used in Cosmetic Formulations:
In the cosmetic industry, Methyl 4-[3-(dimethylamino)propoxy]benzoate is used as a skin conditioning agent to improve the texture and appearance of the skin, making it a popular component in various skincare products.
Used in Fragrance Industry:
Methyl 4-[3-(dimethylamino)propoxy]benzoate is used as a fragrance ingredient in perfumes and other scented products, adding to their aromatic profiles while also offering some UV protection benefits.

Check Digit Verification of cas no

The CAS Registry Mumber 190660-97-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,0,6,6 and 0 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 190660-97:
(8*1)+(7*9)+(6*0)+(5*6)+(4*6)+(3*0)+(2*9)+(1*7)=150
150 % 10 = 0
So 190660-97-0 is a valid CAS Registry Number.

190660-97-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl 4-[3-(dimethylamino)propoxy]benzoate

1.2 Other means of identification

Product number -
Other names methyl 4-[3-(N,N-dimethylamino)-1-propyloxy]benzoate

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:190660-97-0 SDS

190660-97-0Relevant academic research and scientific papers

Light-Promoted Nickel Catalysis: Etherification of Aryl Electrophiles with Alcohols Catalyzed by a NiII-Aryl Complex

Cao, Rui,Lai, Chu-Hui,Li, Gang,Liu, Fengyi,Lu, Huan-Huan,Wang, Chao,Xiao, Jianliang,Xue, Dong,Yang, Liu,Zhang, Wei

supporting information, p. 12714 - 12719 (2020/06/02)

A highly effective C?O coupling reaction of (hetero)aryl electrophiles with primary and secondary alcohols is reported. Catalyzed by a NiII-aryl complex under long-wave UV (390–395 nm) irradiation in the presence of a soluble amine base without any additional photosensitizer, the reaction enables the etherification of aryl bromides and aryl chlorides as well as sulfonates with a wide range of primary and secondary aliphatic alcohols, affording synthetically important ethers. Intramolecular C?O coupling is also possible. The reaction appears to proceed via a NiI–NiIII catalytic cycle.

Semiheterogeneous Dual Nickel/Photocatalytic (Thio)etherification Using Carbon Nitrides

Cavedon, Cristian,Madani, Amiera,Seeberger, Peter H.,Pieber, Bartholom?us

supporting information, p. 5331 - 5334 (2019/07/08)

A carbon nitride material can be combined with homogeneous nickel catalysts for light-mediated cross-couplings of aryl bromides with alcohols under mild conditions. The metal-free heterogeneous semiconductor is fully recyclable and couples a broad range of electron-poor aryl bromides with primary and secondary alcohols as well as water. The application for intramolecular reactions and the synthesis of active pharmaceutical ingredients was demonstrated. The catalytic protocol is applicable for the coupling of aryl iodides with thiols as well.

2-OXO-3,4-DIHYDROPYRIDINE-5-CARBOXYLATES AND THEIR USE

-

Page/Page column 132, (2016/04/20)

The present invention is directed to novel compounds of Formula (I), pharmaceutically acceptable salts or solvates thereof, and their use.

Tec Kinase Inhibitors

-

Page/Page column 12, (2008/12/04)

Disclosed are compounds of formula (I): wherein Q, R1, R2, R3, R4 and R5 are defined herein. The compounds of the invention inhibit Itk kinase and are therefore useful for treating diseases and pathological conditions involving inflammation, immunological disorders and allergic disorders. Also disclosed are processes for preparing these compounds and to pharmaceutical compositions comprising these compounds.

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