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3916-64-1

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3916-64-1 Usage

General Description

2,4-Heptadien-6-one is a chemical compound with the molecular formula C7H8O and a molecular weight of 108.14 g/mol. It is a yellow liquid at room temperature and is primarily used as a fragrance ingredient in the manufacturing of perfumes and other personal care products. 2,4-HEPTADIEN-6-ONE is a 7-carbon saturated and unsaturated ketone, with two conjugated double bonds in its carbon chain. It is also used as a flavoring agent in the food industry and as a chemical intermediate in the synthesis of other organic compounds. Additionally, 2,4-heptadien-6-one is known for its potential use as a chemical building block in the production of pharmaceuticals and agrochemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 3916-64-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,9,1 and 6 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 3916-64:
(6*3)+(5*9)+(4*1)+(3*6)+(2*6)+(1*4)=101
101 % 10 = 1
So 3916-64-1 is a valid CAS Registry Number.
InChI:InChI=1/C7H10O/c1-3-4-5-6-7(2)8/h3-6H,1-2H3/b4-3+,6-5+

3916-64-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4-Heptadien-6-one

1.2 Other means of identification

Product number -
Other names 3,5-Heptadien-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:3916-64-1 SDS

3916-64-1Relevant articles and documents

Br?nsted Base Catalyzed One-Pot Synthesis of Stereodefined Six-Member Carbocycles Featuring Transient Trienolates and a Key Intramolecular 1,6-Addition

Olaizola, Olatz,Iriarte, Igor,Zanella, Giovanna,Gómez-Bengoa, Enrique,Ganboa, I?aki,Oiarbide, Mikel,Palomo, Claudio

supporting information, p. 14250 - 14254 (2019/09/13)

A catalyst-driven one-pot reaction sequence is developed for the enantio- and diastereoselective synthesis of tetrasubstituted cyclohexenes from simple unsaturated ketones or thioesters. The method involves a tertiary amine/squaramide-catalyzed α-selective addition of transiently generated trienolates to nitroolefins, subsequent base-catalyzed double bond isomerization, and an intramolecular (vinylogous) 1,6-addition reaction, a rare key carbocyclization step that proceeded with essentially perfect stereocontrol.

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