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17275-73-9

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17275-73-9 Usage

Description

2-Furanmethanol, a-methyl-a-(phenylmethyl)-, also known as Phenethylfurane, is a synthetic organic compound characterized by its colorless liquid form and a sweet, somewhat floral odor. It is widely recognized for its applications in the flavor and fragrance industry due to its unique aromatic properties.
Used in Food and Beverage Industry:
2-Furanmethanol, a-methyl-a-(phenylmethyl)is used as a flavoring agent for enhancing the taste and aroma of various food and beverage products. Its sweet and floral notes contribute to creating a more appealing and complex flavor profile, making it a valuable ingredient in the culinary world.
Used in Perfumery and Fragrance Industry:
In the perfumery and fragrance industry, 2-Furanmethanol, a-methyl-a-(phenylmethyl)is utilized as a key ingredient for creating unique and captivating scents. Its ability to impart a sweet and floral aroma makes it an essential component in the formulation of perfumes, colognes, and other scented products, adding depth and complexity to the overall fragrance.
Used in Cosmetics and Personal Care Products:
2-Furanmethanol, a-methyl-a-(phenylmethyl)also finds application in the cosmetics and personal care industry, where it is employed to add pleasant and attractive scents to products such as soaps, shampoos, lotions, and creams. Its use in these products not only improves the sensory experience for consumers but also contributes to the overall appeal and marketability of the products.
Used in Aromatherapy:
Due to its sweet and floral aroma, 2-Furanmethanol, a-methyl-a-(phenylmethyl)is also used in aromatherapy as a component of essential oil blends. It can be used to create relaxing and uplifting atmospheres, promoting a sense of well-being and enhancing the therapeutic effects of aromatherapy sessions.

Check Digit Verification of cas no

The CAS Registry Mumber 17275-73-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,2,7 and 5 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 17275-73:
(7*1)+(6*7)+(5*2)+(4*7)+(3*5)+(2*7)+(1*3)=119
119 % 10 = 9
So 17275-73-9 is a valid CAS Registry Number.

17275-73-9SDS

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 1-phenyl-2-furylpropan-2-ol

1.2 Other means of identification

Product number -
Other names 2-[2]furyl-1-phenyl-propan-2-ol

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:17275-73-9 SDS

17275-73-9Downstream Products

17275-73-9Relevant articles and documents

Aldehydes as alkyl carbanion equivalents for additions to carbonyl compounds

Wang, Haining,Dai, Xi-Jie,Li, Chao-Jun

, p. 374 - 378 (2017/04/03)

Nucleophilic addition reactions of organometallic reagents to carbonyl compounds for carbon-carbon bond construction have played a pivotal role in modern chemistry. However, this reaction's reliance on petroleum-derived chemical feedstocks and a stoichiometric quantity of metal have prompted the development of many carbanion equivalents and catalytic metal alternatives. Here, we show that naturally occurring carbonyls can be used as latent alkyl carbanion equivalents for additions to carbonyl compounds, via reductive polarity reversal. Such 'umpolung' reactivity is facilitated by a ruthenium catalyst and diphosphine ligand under mild conditions, delivering synthetically valuable secondary and tertiary alcohols in up to 98% yield. The unique chemoselectivity exhibited by carbonyl-derived carbanion equivalents is demonstrated by their tolerance to protic reaction media and good functional group compatibility. Enantioenriched tertiary alcohols can also be accessed with the aid of chiral ligands, albeit with moderate stereocontrol. Such carbonyl-derived carbanion equivalents are anticipated to find broad utility in chemical bond formation.

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