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(3-aminopropoxy)acetic acid, also known as 3-aminopropoxyacetic acid, is an organic compound with the molecular formula C5H11NO3. It features an amino group and a carboxylic acid group, making it a versatile building block for various chemical products and reactions.

61108-70-1

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61108-70-1 Usage

Uses

Used in Pharmaceutical Production:
(3-aminopropoxy)acetic acid is used as an intermediate in the synthesis of pharmaceuticals for its ability to form key structural components in drug molecules.
Used in Agrochemical Production:
(3-aminopropoxy)acetic acid serves as a precursor in the creation of agrochemicals, contributing to the development of products that enhance crop protection and yield.
Used in Organic Compound Synthesis:
(3-aminopropoxy)acetic acid is utilized as a reagent in chemical reactions, facilitating the synthesis of a wide range of organic compounds for diverse applications.
Used in Chemical Research:
As a building block, (3-aminopropoxy)acetic acid aids in the exploration and development of new chemical entities for various scientific and industrial purposes.
Used in Industrial Applications:
This versatile compound finds use in multiple industries, including but not limited to pharmaceuticals, agrochemicals, and chemical manufacturing, due to its unique structural properties and reactivity.

Check Digit Verification of cas no

The CAS Registry Mumber 61108-70-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,1,0 and 8 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 61108-70:
(7*6)+(6*1)+(5*1)+(4*0)+(3*8)+(2*7)+(1*0)=91
91 % 10 = 1
So 61108-70-1 is a valid CAS Registry Number.

61108-70-1SDS

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 2-(3-aminopropoxy)acetic 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:61108-70-1 SDS

61108-70-1Downstream Products

61108-70-1Relevant academic research and scientific papers

SYNTHESIS OF AZA-CROWN COMPOUNDS BY INTRAMOLECULAR CYCLIZATION OF ω-AMINO ACIDS

Mikhura, I. V.,Formanovskii, A. A.

, p. 205 - 212 (2007/10/02)

A method for the synthesis of aza-crown compounds by the intramolecular cyclization of ω-amino acids with subsequent reduction of the lactam to a macrocyclic amine was developed. 1,8-Diazacyclotetradecane and 1,8-dioxa-4,11-diazacyclotetradecane was synthesized in preparative yields.The structural assignments were made using the IR, 1H and 13C NMR, and mass spectra.

Oxacaprolactams

-

, (2008/06/13)

3-OXACAPROLACTAM IS PREPARED BY A PROCESS WHICH COMPRISES: CONTACTING AN ORGANIC ACID ANHYDRIDE SOLUTION OF A CYANOALKOXYALKANOATE WITH HYDROGEN IN THE PRESENCE OF A NOBLE METAL HYDROGENATION CATALYST TO PREPARE AN AMIDE-ESTER; AND HEATING THE AMIDE-ESTER IN EXCESS WATER AT A TEMPERATURE ABOVE ABOUT 200° C.

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