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4586-97-4

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4586-97-4 Usage

General Description

The chemical compound "(3E,5E,7E,9E,11E,13E,15E,17E)-3,7,12,16-Tetramethyl-18-(2,6,6-trimethyl-1-cyclohexen-1-yl)-3,5,7,9,11,13,15,17-octadecaocten-2-one" is a long-chain, highly unsaturated ketone. It contains a total of 18 carbon atoms, with eight double bonds spaced evenly throughout the molecule. The presence of numerous double bonds makes this compound highly reactive and prone to oxidation. It is also highly lipophilic and is often used in the formulation of cosmetics and personal care products as a fragrance ingredient. Additionally, it has potential applications in the field of organic synthesis for the preparation of various compounds. Due to its complex structure and reactivity, this compound requires careful handling and storage.

Check Digit Verification of cas no

The CAS Registry Mumber 4586-97-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,5,8 and 6 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4586-97:
(6*4)+(5*5)+(4*8)+(3*6)+(2*9)+(1*7)=124
124 % 10 = 4
So 4586-97-4 is a valid CAS Registry Number.

4586-97-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (all-E)-sintaxanthin

1.2 Other means of identification

Product number -
Other names Sintoxanthin

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:4586-97-4 SDS

4586-97-4Downstream Products

4586-97-4Relevant articles and documents

Total Synthesis of C31-Methyl Ketone Apocarotenoids: Sintaxanthin and (3R)-3-Hydroxysintaxanthin

Haugan, Jarle Andre

, p. 657 - 664 (2007/10/02)

The previously undescribed (all-E)-2,7,11-trimethyl-12-oxo-2,4,6,8,10-tridecapentenal has been synthesised in 26percent overall yield in six steps from the readily available 3-methyl-2-penten-4-yn-1-ol and 2,7-dimethyl-2,4,6-octatrienedial.This C16-keto aldehyde was used in the first total synthesis of fully characterised (all-E)-sintaxanthin and optically active (all-E)-(3R)-3-hydroxysintaxanthin.The C16-keto aldehyde is a versatile building block for any C31-methyl ketone apocarotenoid.

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