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METHYL 2-(AMINOMETHYL)-3-FUROATE, with the molecular formula C7H9NO3, is a chemical compound derived from furoic acid. It features a methyl group and an amino group attached to the furoate ring, which endows it with a range of potential applications in various fields.

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  • 306936-50-5 Structure
  • Basic information

    1. Product Name: METHYL 2-(AMINOMETHYL)-3-FUROATE
    2. Synonyms: METHYL 2-(AMINOMETHYL)-3-FUROATE;BUTTPARK 147\50-38;3-Furancarboxylicacid,2-(aminomethyl)-,methylester(9CI);3-Furancarboxylic acid,2-(aminomethyl)-, methyl ester
    3. CAS NO:306936-50-5
    4. Molecular Formula: C7H9NO3
    5. Molecular Weight: 155.15
    6. EINECS: N/A
    7. Product Categories: CARBOXYLICESTER
    8. Mol File: 306936-50-5.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 261.7°Cat760mmHg
    3. Flash Point: 112°C
    4. Appearance: /
    5. Density: 1.192g/cm3
    6. Vapor Pressure: 0.0114mmHg at 25°C
    7. Refractive Index: 1.507
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. PKA: 8.31±0.29(Predicted)
    11. CAS DataBase Reference: METHYL 2-(AMINOMETHYL)-3-FUROATE(CAS DataBase Reference)
    12. NIST Chemistry Reference: METHYL 2-(AMINOMETHYL)-3-FUROATE(306936-50-5)
    13. EPA Substance Registry System: METHYL 2-(AMINOMETHYL)-3-FUROATE(306936-50-5)
  • Safety Data

    1. Hazard Codes: Xi
    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: 306936-50-5(Hazardous Substances Data)

306936-50-5 Usage

Uses

Used in Pharmaceutical Industry:
METHYL 2-(AMINOMETHYL)-3-FUROATE is used as a building block for the synthesis of various bioactive molecules. Its unique structure allows it to be a key component in the development of new pharmaceutical compounds, contributing to advancements in medicinal chemistry.
Used in Fragrance Industry:
In the fragrance industry, METHYL 2-(AMINOMETHYL)-3-FUROATE is utilized as a flavoring agent and fragrance ingredient. Its distinct chemical properties enable it to impart specific scents and flavors to various products, enhancing their sensory appeal.
Used in Antimicrobial Applications:
METHYL 2-(AMINOMETHYL)-3-FUROATE has been studied for its potential antimicrobial properties. It can be employed as an antimicrobial agent in various applications, such as in the development of disinfectants, sanitizers, and preservatives, to inhibit the growth of harmful microorganisms.
Used in Antifungal Applications:
Similarly, METHYL 2-(AMINOMETHYL)-3-FUROATE has shown promise as an antifungal agent. It can be used in the formulation of antifungal products, such as creams, sprays, and powders, to treat and prevent fungal infections.
Overall, METHYL 2-(AMINOMETHYL)-3-FUROATE is a versatile chemical compound with a wide range of potential applications in the pharmaceutical, fragrance, antimicrobial, and antifungal industries. Its unique structure and properties make it a valuable asset for the development of innovative products and solutions in these fields.

Check Digit Verification of cas no

The CAS Registry Mumber 306936-50-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,6,9,3 and 6 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 306936-50:
(8*3)+(7*0)+(6*6)+(5*9)+(4*3)+(3*6)+(2*5)+(1*0)=145
145 % 10 = 5
So 306936-50-5 is a valid CAS Registry Number.
InChI:InChI=1/C7H9NO3/c1-10-7(9)5-2-3-11-6(5)4-8/h2-3H,4,8H2,1H3

306936-50-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 2-(aminomethyl)furan-3-carboxylate

1.2 Other means of identification

Product number -
Other names Methyl 2-(Aminomethyl)-3-Furoate

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:306936-50-5 SDS

306936-50-5Downstream Products

306936-50-5Relevant articles and documents

A novel class of compounds: Synthesis of 5,5′-carbonyl-bis(5,6- dihydro-4H-furo- and thieno-[2,3-c]pyrrol-4-ones)

Koza, Gani,Balci, Metin

, p. 8679 - 8684 (2011)

We hereby report the first synthesis of novel class of compounds, 5,5′-carbonyl-bis(5,6-dihydro-4H-thieno- and furo-[2,3-c]pyrrol-4-one starting from methyl 2-(2-methoxy-2-oxoethyl) thiophene- and furan-3-carboxylate, respectively. The ester functionalities connected to methylene group were regiospecifically converted to the desired monoacyl azides. Curtius rearrangement of acyl azides followed by hydrolysis of the formed isocyanates gave the symmetrical urea derivatives. Cyclization of the ester groups provided the target compounds.

Regioselective synthesis of the 5,6-dihydro-4H-furo[2,3-c]pyrrol-4-one skeleton: A new class of compounds

Koza, Gani,Karahan, Emrah,Balci, Metin

experimental part, p. 1698 - 1704 (2010/12/20)

We hereby report the first preparation of the 5,6-dihydro-4H-furo[2,3-c] pyrrol-4-one (3) and its derivatives starting from methyl 3-(methoxycarbonyl) furan-2-acetate (8). The ester functionality connected to the methylene group was regiospecifically conv

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