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3506-88-5

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3506-88-5 Usage

General Description

3-Benzyl-4-phenyl-2-butanone is a chemical compound with the molecular formula C18H18O. It is a ketone compound that belongs to the class of organic compounds known as ketones. This chemical is a yellowish liquid with a sweet, floral odor, and is commonly used in the fragrance and flavor industry. It is also used in the production of perfumes, soaps, and cosmetics due to its pleasant and long-lasting scent. In addition, 3-benzyl-4-phenyl-2-butanone has been found to exhibit antimicrobial and antioxidant properties, making it a versatile compound with various industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 3506-88-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,0 and 6 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3506-88:
(6*3)+(5*5)+(4*0)+(3*6)+(2*8)+(1*8)=85
85 % 10 = 5
So 3506-88-5 is a valid CAS Registry Number.
InChI:InChI=1/C17H18O/c1-14(18)17(12-15-8-4-2-5-9-15)13-16-10-6-3-7-11-16/h2-11,17H,12-13H2,1H3

3506-88-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-benzyl-4-phenylbutan-2-one

1.2 Other means of identification

Product number -
Other names 3-benzyl-4-phenyl-butan-2-one

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:3506-88-5 SDS

3506-88-5Relevant articles and documents

Catalyst-Free Decarboxylative Fluorination of Tertiary β-Keto Carboxylic Acids

Katada, Misaki,Kitahara, Kazumasa,Iwasa, Seiji,Shibatomi, Kazutaka

supporting information, p. 2408 - 2411 (2018/11/23)

Decarboxylative fluorination of tertiary β-keto carboxylic acids was performed using an electrophilic fluorinating reagent. The reaction proceeded in the absence of a catalyst or base to yield the corresponding α-fluoroketones with tertiary fluorocarbons in good to high yields. Considering that the α-fluorination of asymmetrical ketones often causes problems with the regioselectivity between the α- and α′-positions, this method could be a good alternative to the α-fluorination of simple ketones for the synthesis of tertiary fluoroketones.

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