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CAS

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34841-03-7

3-Amino-3-(3,4-dimethoxy-phenyl)-propionic acid methyl ester hydrochloride is a chemical compound with the molecular formula C12H18ClNO5. It is a derivative of 3-amino-3-phenylpropionic acid, featuring a 3,4-dimethoxyphenyl group attached to the phenyl ring and a methyl ester group at the carboxylic acid position. 3-AMINO-3-(3,4-DIMETHOXY-PHENYL)-PROPIONIC ACID METHYL ESTER HYDROCHLORIDE is known for its potential applications in pharmaceuticals and as an intermediate in the synthesis of various drugs. It is characterized by its hydrochloride salt form, which contributes to its stability and solubility properties. The compound's structure and functional groups make it a versatile building block in organic chemistry and medicinal chemistry, particularly in the development of compounds with potential therapeutic effects.

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  • 3-AMINO-3-(3,4-DIMETHOXY-PHENYL)-PROPIONIC ACID METHYL ESTER HYDROCHLORIDE

    Cas No: 34841-03-7

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  • 34841-03-7 Structure

  • Basic information

    1. Product Name: 3-AMINO-3-(3,4-DIMETHOXY-PHENYL)-PROPIONIC ACID METHYL ESTER HYDROCHLORIDE
    2. Synonyms: METHYL 3-AMINO-3-(3,4-DIMETHOXYPHENYL)PROPANOATE HYDROCHLORIDE;3-AMINO-3-(3,4-DIMETHOXY-PHENYL)-PROPIONIC ACID METHYL ESTER HCL;3-AMINO-3-(3,4-DIMETHOXY-PHENYL)-PROPIONIC ACID METHYL ESTER HYDROCHLORIDE
    3. CAS NO:34841-03-7
    4. Molecular Formula: C12H18ClNO4
    5. Molecular Weight: 275.73
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 34841-03-7.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 3-AMINO-3-(3,4-DIMETHOXY-PHENYL)-PROPIONIC ACID METHYL ESTER HYDROCHLORIDE(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-AMINO-3-(3,4-DIMETHOXY-PHENYL)-PROPIONIC ACID METHYL ESTER HYDROCHLORIDE(34841-03-7)
    11. EPA Substance Registry System: 3-AMINO-3-(3,4-DIMETHOXY-PHENYL)-PROPIONIC ACID METHYL ESTER HYDROCHLORIDE(34841-03-7)

  • Safety Data

    1. Hazard Codes: Xn
    2. Statements: 22
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: IRRITANT
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 34841-03-7(Hazardous Substances Data)

34841-03-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 34841-03-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,8,4 and 1 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 34841-03:
(7*3)+(6*4)+(5*8)+(4*4)+(3*1)+(2*0)+(1*3)=107
107 % 10 = 7
So 34841-03-7 is a valid CAS Registry Number.

34841-03-7Relevant articles and documents

ISOINDOLE DERIVATIVE

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Paragraph 0229; 0235, (2021/02/25)

Disclosed is a compound of formula (I) and a stereoisomer thereof: wherein R1, R2, R3 and R4 are as defined in the present disclosure.

Facile synthesis of N-(9-fluorenylmethyloxycarbonyl)-3-amino-3-(4,5- dimethoxy-2-nitrophenyl)propionic acid as a photocleavable linker for solid-phase peptide synthesis

Kim, Jaehi,Kyeong, San,Shin, Dong-Sik,Yeo, Sewon,Yim, Joonhyuk,Lee, Yoon-Sik

, p. 733 - 736 (2013/05/09)

A photocleavable linker, N-(9-fluorenylmethyloxycarbonyl)-3-amino-3-(4,5- dimethoxy-2-nitrophenyl)propionic acid was synthesized from veratraldehyde, with simple reaction and separation steps. This linker was stable under the normal solid-phase peptide sy

METHODS OF USING AND COMPOSITIONS COMPRISING (+)-3-(3,4-DIMETHOXY-PHENYL)-3-(1-OXO-1,3-DIHYDRO-ISOINDOL-2-YL)-PROPIONAMIDE

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Page/Page column 32; 38, (2008/06/13)

Enantiomerically pure (+)-3 -(3,4-dimethoxy-phenyl)-3-(1-oxo-1,3-dihydro-isoindol-2-yl)-propionamide, and prodrugs, metabolites, polymorphs, salts, solvates (e.g., hydrates), and clathrates thereof are discussed. Methods of treating and/or preventing vari

Cyclic amides

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, (2008/06/13)

Cyclic amides are inhibitors of tumor necrosis factor and can be used to combat cachexia, endotoxic shock, and retrovirus replication. A typical embodiment is 3-phenyl-3-(1-oxoisoindolin-2-yl)propionamide.

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