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4-[(2-HYDROXY-ETHYL)-METHYL-AMINO]-BENZOIC ACID is a chemical compound with the molecular formula C11H15NO4. It is a derivative of benzoic acid, featuring a hydroxyl group and a methylamino group attached to the benzene ring. 4-[(2-HYDROXY-ETHYL)-METHYL-AMINO]-BENZOIC ACID plays a significant role as a pharmaceutical intermediate and holds potential for use in the synthesis of drugs and other organic compounds. Its unique properties and applications make it a valuable chemical in the fields of medicine and organic chemistry.
Used in Pharmaceutical Industry:
4-[(2-HYDROXY-ETHYL)-METHYL-AMINO]-BENZOIC ACID is used as a pharmaceutical intermediate for its ability to be a key component in the development and synthesis of various drugs. Its structural features allow it to be a versatile building block in medicinal chemistry, contributing to the creation of new therapeutic agents.
Used in Organic Chemistry:
In the realm of organic chemistry, 4-[(2-HYDROXY-ETHYL)-METHYL-AMINO]-BENZOIC ACID is utilized as a synthetic intermediate. Its presence in chemical reactions can lead to the formation of a wide range of organic compounds, making it an essential component in the synthesis of various chemical products.

769132-75-4

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769132-75-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 769132-75-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,6,9,1,3 and 2 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 769132-75:
(8*7)+(7*6)+(6*9)+(5*1)+(4*3)+(3*2)+(2*7)+(1*5)=194
194 % 10 = 4
So 769132-75-4 is a valid CAS Registry Number.
InChI:InChI=1/C10H13NO3/c1-11(6-7-12)9-4-2-8(3-5-9)10(13)14/h2-5,12H,6-7H2,1H3,(H,13,14)

769132-75-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[2-hydroxyethyl(methyl)amino]benzoic acid

1.2 Other means of identification

Product number -
Other names -

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:769132-75-4 SDS

769132-75-4Downstream Products

769132-75-4Relevant academic research and scientific papers

Direct hydroxyethylation of amines by carbohydrates: Via ruthenium catalysis

Jia, Le,Makha, Mohamed,Du, Chen-Xia,Quan, Zheng-Jun,Wang, Xi-Cun,Li, Yuehui

supporting information, p. 3127 - 3132 (2019/06/18)

An efficient and halogen-free catalytic methodology for the synthesis of β-amino alcohols from aromatic amines and biomass-derived carbohydrates is demonstrated for the first time. The activation of C5/C6 sugars by a ruthenium catalyst selectively generates the C2 alkylating reagent glycolaldehyde. The transformation involves metal-catalyzed hydrogen borrowing for the reduction of the imine intermediate. A series of arylamines bearing various substituents were successfully transformed into the desired products in good to excellent yields.

FUSED QUINOLINE DERIVATIVE AND USE THEREOF

-

, (2008/06/13)

The present invention aims at provision of a quinoline derivative having a neurokinin 2 (NK2) receptor antagonistic action and relates to a compound represented by the formula (I) wherein Rl is a hydrogen atom and the like; R2 is a hydrogen atom, a hydrocarbon group optionally having substituent(s) and the like; R3 is unsubstituted (i.e., absence), a hydrogen atom and the like; R4 and R5 are the same or different and each is a hydrogen atom, a hydrocarbon group optionally having substituent(s), and the like; R6is (cyclic group optionally having substituent(s)) -carbonyl, and the like; R7, R8,R9 and R10 are the same or different and each is a hydrogen atom, halogen and the like; or R7and R8,R8 and R9,and R9 and R10 may form a ring together with the adjacent carbon atoms; n is an integer of 1 to 5; --- represents unsubstituted (i.e., absence) or a single bond; and --- represents a single bond or a double bond, or a salt thereof, and the like.

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