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147159-48-6

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147159-48-6 Usage

Also Known As

(E)-6-decenal

Chemical Class

Aldehyde

Physical State

Colorless liquid

Odor

Strong, citrus-like

Natural Sources

Found in essential oils, particularly citrus fruits like oranges and lemons

Uses in Food Industry

Flavoring agent in food products

Uses in Cosmetics

Fragrance in perfumes and cosmetics

Industrial Applications

Used in the production of soaps and detergents

Antimicrobial Properties

Exhibits antimicrobial properties

Health Benefits

Potential antioxidant and anti-inflammatory properties

Check Digit Verification of cas no

The CAS Registry Mumber 147159-48-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,7,1,5 and 9 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 147159-48:
(8*1)+(7*4)+(6*7)+(5*1)+(4*5)+(3*9)+(2*4)+(1*8)=146
146 % 10 = 6
So 147159-48-6 is a valid CAS Registry Number.

147159-48-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (E)-6-decenal

1.2 Other means of identification

Product number -
Other names dec-6t-enal

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:147159-48-6 SDS

147159-48-6Downstream Products

147159-48-6Relevant articles and documents

Towards a biomimetic synthesis of the marine alkaloids papuamine and haliclonadiamine: Model studies

Adlington, Robert M.,Baldwin, Jack E.,Challis, Gregory L.,Cox, Rhona J.,Pritchard, Gareth J.

, p. 623 - 628 (2000)

A plausible biosynthetic pathway for the isomeric marine alkaloids papuamine and haliclonadiamine via the double tandem ene cyclisation of a tetraenediimine is proposed. Initial model studies directed toward the biomimetic synthesis of these alkaloids are

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