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141545-99-5

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141545-99-5 Usage

Description

2-benzyl-1-(3,4-dimethoxyphenyl)-2-(dimethylamino)butan-1-onato(2-) is a complex organic compound characterized by its unique structure, which includes a benzyl group, a 3,4-dimethoxyphenyl moiety, and a dimethylamino butan-1-onato(2-) bridge. As a derivative of 3,4-dimethoxyphenyl and dimethylamino butan-1-onato, this compound may offer potential applications in various fields, pending further research and validation of its properties and utility.

Uses

Given the provided materials, the specific uses of 2-benzyl-1-(3,4-dimethoxyphenyl)-2-(dimethylamino)butan-1-onato(2-) are not explicitly detailed. However, based on its chemical structure and the general properties of similar compounds, we can hypothesize potential applications in the following industries:
Used in Pharmaceutical Industry:
2-benzyl-1-(3,4-dimethoxyphenyl)-2-(dimethylamino)butan-1-onato(2-) could be used as a pharmaceutical intermediate for the synthesis of drugs targeting various therapeutic areas. Its unique structure may allow for the development of novel compounds with specific biological activities, such as analgesics, anti-inflammatory agents, or central nervous system modulators.
Used in Chemical Research:
In the field of chemical research, 2-benzyl-1-(3,4-dimethoxyphenyl)-2-(dimethylamino)butan-1-onato(2-) may serve as a starting material or a building block for the synthesis of more complex organic molecules. Its reactivity and functional groups could be exploited in organic synthesis to create new compounds with potential applications in various industries.
Used in Material Science:
2-benzyl-1-(3,4-dimethoxyphenyl)-2-(dimethylamino)butan-1-onato(2-) may also find use in material science, particularly in the development of new polymers or materials with specific properties. The presence of the benzyl and dimethylamino groups could influence the compound's solubility, stability, or reactivity, making it a candidate for use in the creation of advanced materials with tailored characteristics.

Check Digit Verification of cas no

The CAS Registry Mumber 141545-99-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,5,4 and 5 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 141545-99:
(8*1)+(7*4)+(6*1)+(5*5)+(4*4)+(3*5)+(2*9)+(1*9)=125
125 % 10 = 5
So 141545-99-5 is a valid CAS Registry Number.

141545-99-5Upstream product

141545-99-5Downstream Products

141545-99-5Relevant articles and documents

Oxygen-containing titanocenes, and the use thereof

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, (2008/06/13)

Titanocenes of the formula I STR1 in which R1 are cyclopentadienyl? groups and R2 and R3 are aromatic radicals which are substituted in both ortho-positions by fluorine and, in addition, are substituted by an acyloxy group are suitable as photoinitiators for the photopolymerization of ethylenically unsaturated compounds.

Novel alpha-aminoacetophenones as photoinitiators

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, (2008/06/13)

Compounds of the formula I, II, III and IIIa STR1 in which Ar1 is an unsubstituted or substituted aromatic radical and at least one of the radicals R1 and R2 is an alkenyl, cycloalkenyl or arylmethyl group, are effective photoinitiators for photopolymerization of unsaturated compounds. They are particularly suitable for photocuring of pigmented systems.

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