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3,5-Heptadien-2-one, (E,Z)- is an organic compound with the molecular formula C7H10O. It is a colorless liquid with a strong, pungent odor. This chemical is a conjugated diene, which means it has two carbon-carbon double bonds separated by a single bond. The (E,Z) notation indicates the geometric configuration of the double bonds, with the E (entgegen) and Z (zusammen) prefixes describing the relative positions of the substituents on the double-bonded carbons. 3,5-Heptadien-2-one is used as a synthetic intermediate in the production of various chemicals, including fragrances and pharmaceuticals. It is also known for its potential applications in the synthesis of natural products and as a building block in organic chemistry. Due to its reactivity, it is important to handle 3,5-Heptadien-2-one, (E,Z)- (8CI,9CI) with care, following appropriate safety protocols.

4173-40-4

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4173-40-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4173-40-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,1,7 and 3 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 4173-40:
(6*4)+(5*1)+(4*7)+(3*3)+(2*4)+(1*0)=74
74 % 10 = 4
So 4173-40-4 is a valid CAS Registry Number.

4173-40-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name heptadiene-3,5 one-2 (3E,5Z)

1.2 Other means of identification

Product number -
Other names (3E,5Z)-Hepta-3,5-dien-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:4173-40-4 SDS

4173-40-4Downstream Products

4173-40-4Relevant academic research and scientific papers

ACTION DES COMPOSES ORGANOMAGNESIENS SUR LES PYRONES-2 - VII ETUDE DE LA STABILITE RELATIVE DES HYDROXY-6 DYHIDRO-5,6 2H-PYRANNES ET DES CETOLS TAUTOMERES CORRESPONDANTS

Lhoste, P.,Moreau, M.,Dreux, J.

, p. 1551 - 1562 (2007/10/02)

In the reaction between organomagnesium compounds and 2-pyrones, the relative stability of the 6-hydroxy 5,6 2H-pyrans and their tautomeric forms (ketols) has no influence on the reaction pathway.When ethylenic ketols are obtained, the corresponding tautomeric dihydropyranols are prepared in a selective way by reaction of nucleophilic reagents on the 3,6-dihydropyrones.In the other hand, the exclusive formation either of the dihydropyranols or of the unsatured ketols E, during these two reactions, shows up that here is no equilibrium between these two entities in the experimental conditions.

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