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CAS

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149692-49-9

3-[benzyl(methyl)amino]propanoic acid, also known as benzyldimethylaminoacetic acid, is a unique amino acid derivative belonging to the propanoic acid class. It features a benzyl group attached to the amino group at the third position, which, along with the methyl group, endows the compound with distinctive properties. This chemical is predominantly utilized in the synthesis of pharmaceuticals and serves as a reagent in organic chemistry, although its potential hazards and toxicity necessitate careful handling.

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  • 149692-49-9 Structure

  • Basic information

    1. Product Name: 3-[benzyl(methyl)amino]propanoic acid
    2. Synonyms: 3-[benzyl(methyl)amino]propanoic acid;N-Benzyl-N-methyl-beta-alanine;3-(benzyl-methyl-amino)propionic acid;3-(methyl-(phenylmethyl)amino)propanoic acid
    3. CAS NO:149692-49-9
    4. Molecular Formula: C11H15NO2
    5. Molecular Weight: 193.2423
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 149692-49-9.mol

  • Chemical Properties

    1. Melting Point: 112-112.5 °C
    2. Boiling Point: 310.9±25.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.112±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: Sealed in dry,Room Temperature
    8. Solubility: N/A
    9. PKA: 3.66±0.14(Predicted)
    10. CAS DataBase Reference: 3-[benzyl(methyl)amino]propanoic acid(CAS DataBase Reference)
    11. NIST Chemistry Reference: 3-[benzyl(methyl)amino]propanoic acid(149692-49-9)
    12. EPA Substance Registry System: 3-[benzyl(methyl)amino]propanoic acid(149692-49-9)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 149692-49-9(Hazardous Substances Data)

149692-49-9 Usage

Uses

Used in Pharmaceutical Synthesis:
3-[benzyl(methyl)amino]propanoic acid is used as a key intermediate in the synthesis of various pharmaceuticals for its unique structural properties that facilitate the creation of new drug molecules.
Used in Organic Chemistry as a Reagent:
In the realm of organic chemistry, 3-[benzyl(methyl)amino]propanoic acid is employed as a reagent, leveraging its distinctive chemical characteristics to catalyze or participate in a range of chemical reactions, contributing to the advancement of chemical research and product development.
Used in Chemical Research:
3-[benzyl(methyl)amino]propanoic acid is utilized in chemical research to explore its potential applications and reactions, furthering understanding of its properties and behavior in different chemical contexts.

Check Digit Verification of cas no

The CAS Registry Mumber 149692-49-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,9,6,9 and 2 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 149692-49:
(8*1)+(7*4)+(6*9)+(5*6)+(4*9)+(3*2)+(2*4)+(1*9)=179
179 % 10 = 9
So 149692-49-9 is a valid CAS Registry Number.

149692-49-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N-Benzyl-N-methyl-β-alanine

1.2 Other means of identification

Product number -
Other names 3-(benzyl(methyl)amino)propanoic acid

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:149692-49-9 SDS

149692-49-9Relevant articles and documents

Synthesis method of 3-methylaminopropionic acid

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Paragraph 0008, (2021/01/24)

The invention relates to a synthetic method of 3-methylaminopropionic acid. The method mainly solves the technical problems that the existing method for preparing 3-methylaminopropionic acid has manyreaction steps and is not easy for large-scale productio

Synthesis of 3-(2-aminoethyl)-5-hydroxy-1H-pyrazole derivatives

Groselj, Uros,Kralj, David,Wagger, Jernej,Dahmann, Georg,Stanovnik, Branko,Svete, Jurij

experimental part, p. 49 - 65 (2012/03/11)

Treatment of β-keto ester 8 with hydrazines 9a-g gave 1'-substituted tert-butyl 2-(5-hydroxy-1Hpyrazol- 3-yl)ethylcarbamates 10a-e and 2-(5-oxo-2,5-dihydro-1H-pyrazol-3-yl)ethylcarbamates 11f,g. Acidolytic deprotection of 10b,c afforded the corresponding 3-(2-aminoethyl)-5-hydroxy- 1H-pyrazoles 6b,c in good yields. Acylation of 6 gave either the N-acyl compounds 12b,c and 13c, or the N,O-diacyl derivative 14. Next, three N,N-dialkyl analogues 15a,b and 26c were prepared from dimethyl acetone-1,3-dicarboxylate 21 via condensation with hydrazines 9a and 9h followed by hydrolysis of the esters 22a,b, amidation of the carboxylic acids 23a,b, and reduction of the tertiary carboxamides 24a and 25b,c. ARKAT-USA, Inc.

ARYLOXY-AND HETEROARYLOXY-SUBSTITUTED TETRAHYDROBENZAZEPINES AND USE THEREOF TO BLOCK REUPTAKE OF NOREPINEPHRINE, DOPAMINE, AND SEROTONIN

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Page/Page column 87, (2009/01/20)

The aryloxy- and heteroaryloxy-substituted tetrahydrobenzazepine derivative compounds of the present invention are represented by formulae (I) (A-E) having the following structure where the carbon atom designated * is in the R or S configuration and the s

Cerium(IV) oxidations of β-aminoketones, VIII: Synthesis of 1,2,3,4-tetrahydroisoquinolines with differently substituted piperidine parts

Holzgrabe,Inkman

, p. 209 - 215 (2007/10/02)

1- and 3-Alkyl- and/or aryl substituted tetrahydroisoquinolines are obtained by oxidative cyclisation of N-benzyl-β-aminoketones with cerium(IV) sulphate. In nearly all cases formation of mixtures of diastereomeres is observed. If the ketone function is r

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