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4330-24-9

2-furylmethyl 4-methylbenzoate is an organic compound with the chemical formula C12H12O3. It is a derivative of benzoic acid, featuring a furyl group attached to the methyl group on the benzene ring. 2-furylmethyl 4-methylbenzoate is characterized by its unique aroma and is often used in the fragrance industry as a fixative and scent enhancer. It can be synthesized through various chemical reactions, such as the esterification of 4-methylbenzoic acid with 2-furylmethanol. Due to its complex structure, 2-furylmethyl 4-methylbenzoate is a valuable component in the creation of perfumes, cosmetics, and other scented products, contributing to their long-lasting and rich olfactory profiles.

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  • 4330-24-9 Structure

  • Basic information

    1. Product Name: 2-furylmethyl 4-methylbenzoate
    2. Synonyms: 2-furylmethyl 4-methylbenzoate
    3. CAS NO:4330-24-9
    4. Molecular Formula: C13H12O3
    5. Molecular Weight: 216.23258
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 4330-24-9.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: 2-furylmethyl 4-methylbenzoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-furylmethyl 4-methylbenzoate(4330-24-9)
    11. EPA Substance Registry System: 2-furylmethyl 4-methylbenzoate(4330-24-9)

  • 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: 4330-24-9(Hazardous Substances Data)

4330-24-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4330-24-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,3 and 0 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4330-24:
(6*4)+(5*3)+(4*3)+(3*0)+(2*2)+(1*4)=59
59 % 10 = 9
So 4330-24-9 is a valid CAS Registry Number.

4330-24-9Downstream Products

4330-24-9Relevant articles and documents

HMF and furfural: Promising platform molecules in rhodium-catalyzed carbonylation reactions for the synthesis of furfuryl esters and tertiary amides

Qi, Xinxin,Zhou, Rong,Ai, Han-Jun,Wu, Xiao-Feng

, p. 215 - 221 (2019/11/25)

A biomass involved rhodium-catalyzed carbonylative synthesis of furfuryl esters and tertiary amides has been developed. 5-Hydroxymethylfurfural (HMF) was used as both substrate and CO surrogate for the first time in a carbonylation reaction, and both alkyl and aryl iodides were tolerated well to afford the desired furfuryl esters in moderate to good yields. In addition, furfural was also utilized as a CO source for the synthesis of tertiary amides. A variety of tertiary amides were obtained in moderate to excellent yields with good functional groups compatibility. Notably, tertiary amines were used as the amine source through a C[sbnd]N bond cleavage pathway in the absence of additional oxidant.

Sonogashira reactions of α- and β-1-ethynyl-2-deoxyribosides: synthesis of acetylene-extended C-nucleosides

Bobula, Tomá?,Hocek, Michal,Kotora, Martin

supporting information; experimental part, p. 530 - 536 (2010/03/03)

An improved practical protocol for the synthesis of both anomers of 1-ethynyl-2-deoxiribosides 1 was developed. The Sonogashira coupling of ethynyldeoxyribosides 1 with various aryl- and heteroaryl halides was carried out under various conditions. It was

Convenient preparation of 2-deoxy-3,5-di-O-p-toluoyl-α-D-erythro-pentofuranosyl chloride

Rolland, Valerie,Kotera, Mitsuharu,Lhomme, Jean

, p. 3505 - 3511 (2007/10/03)

By using acetyl chloride as HCl generator, the procedure for the Hoffer preparation of the α-chloro sugar 4a was significantly improved. The α-configuration of the chloro atom was confirmed by using NOE measurement. Sequential transformation of 4a to the β-anomer and to the furfuryl derivative 6 was studied.

An efficient method for the synthesis of aromatic C-nucleosides

Chaudhuri, Narayan C.,Kool, Eric T.

, p. 1795 - 1798 (2007/10/02)

Reaction of diarylcadmium or diarylzinc reagents with 1,2-dideoxy-3,5-di-O-p-toluoyl-1-chloro-α-D-ribofuranose affords 3,5-di-O-protected aromatic C-nucleosides in good yields.

Nucleosides, XXXVI. - Synthesis and Properties of 4-Amino-8-β-D-ribofuranosyl-7(8H)-pteridinone and its 2- and 6-Phenyl Derivatives.

Harris, Roger,Pfleiderer, Wolfgang

, p. 1457 - 1468 (2007/10/02)

4-Amino-7(8H)-pteridinone (5) and its 2- and 5-phenyl derivatives (6-8) are converted by the Silyl-Hilbert-Johnson method to the corresponding acylated N-8-ribosides (15-18, 23, 24).Deacylation led to the free pteridine nucleosides (19-22, 25) which can b

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