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4-aminomethylphenylacetic acid ethyl ester is a chemical compound derived from phenylacetic acid, featuring an ethyl ester group, an amino group, a methyl group, and a benzene ring. It serves as an intermediate in the synthesis of pharmaceuticals and agrochemicals and holds potential therapeutic applications as a neurotransmitter precursor.

62910-48-9

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62910-48-9 Usage

Uses

Used in Pharmaceutical Industry:
4-aminomethylphenylacetic acid ethyl ester is used as an intermediate in the synthesis of various pharmaceuticals for its role in creating essential medications.
Used in Agrochemical Industry:
4-aminomethylphenylacetic acid ethyl ester is also utilized as an intermediate in the production of agrochemicals, contributing to the development of agricultural products.
Used in Therapeutic Applications:
4-aminomethylphenylacetic acid ethyl ester is used as a neurotransmitter precursor, indicating its potential in the treatment of neurological conditions and disorders.

Check Digit Verification of cas no

The CAS Registry Mumber 62910-48-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,9,1 and 0 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 62910-48:
(7*6)+(6*2)+(5*9)+(4*1)+(3*0)+(2*4)+(1*8)=119
119 % 10 = 9
So 62910-48-9 is a valid CAS Registry Number.

62910-48-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-[4-(aminomethyl)phenyl]acetate

1.2 Other means of identification

Product number -
Other names Benzeneacetic acid,4-(aminomethyl)-,ethyl ester

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:62910-48-9 SDS

62910-48-9Upstream product

62910-48-9Relevant academic research and scientific papers

Novel thiophene derivatives, their process of preparation and the pharmaceutical compositions which comprise them

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Page/Page column 19, (2010/11/30)

A compound of formula (I) selected from: wherein: X represents oxygen or sulphur, Y represents oxygen, —NH— or —N(C1-C6)alkyl-, Ra represents hydrogen, halogen, (C1-C3)alkyl, hydroxyl or (C1-C3)alkoxy, Rb represents hydrogen, halogen or (C1-C3)alkyl, A represents phenyl, pyridyl, (C5-C6)cycloalkyl or (C5-C6)cycloalkenyl, R1 and R2 each represent a group selected from hydrogen, halogen, cyano, nitro, haloalkyl, haloalkoxy, alkyl, alkenyl, alkynyl, —OR4, —NR4R5, —S(O)nR4, —C(O)R4, —CO2R4, —O—C(O)R4, —C(O)NR4R5, —NR5—C(O)R4, —NR5—SO2R4, -T-CN, -T-OR4, -T-OCF3, -T- NR4R5, -T-S(O)nR4, -T-C(O)R4, -T-CO2R4, -T-O—C(O)R4, -T-C(O)NR4R5, -T-NR4—C(O)R5, -T-NR4—SO2R5, —R6 and -T-R6 in which n, T, R4, R5 and R6 are as defined in the description, R3 represents an —R7 or —U—R11 group in which R7 represents hydrogen, alkyl, aryl, cycloalkyl or heterocycle, U represents a linear or branched alkylene chain and R11 is defined in the description, their optical isomers or their addition salts with a pharmaceutically acceptable acid or base, and their use as inhibitor of metalloproteinase and more specifically of metalloproteinase-12.

NOVEL PYRIMIDINE-4,6-DICARBOXAMIDES FOR THE SELECTIVE INHIBITION OF COLLAGENASES

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Page/Page column 45, (2008/06/13)

Pyrimidine-4,6-dicarboxamides of formula (I), are suitable for the selective inhibition of collagenase (MMP 13). The pyrimidine-4,6-dicarboxamides can thus be used for the treatment of degenerative joint diseases.

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