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(2E)-pentadec-2-enal is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

64462-00-6

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64462-00-6 Usage

Uses

Used in Food Industry:
(2E)-pentadec-2-enal is used as a flavoring agent for its distinctive fruity and floral odor, enhancing the taste and aroma of various food products.
Used in Fragrance Industry:
(2E)-pentadec-2-enal is used as a base or modifier in the production of perfumes and other cosmetic products, contributing to their unique and appealing scents.
Used in Pharmaceutical Industry:
While research is ongoing, (2E)-pentadec-2-enal is being explored for its potential health benefits, such as antioxidant and anti-inflammatory properties, which could lead to its use in pharmaceutical applications.

Check Digit Verification of cas no

The CAS Registry Mumber 64462-00-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,4,6 and 2 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 64462-00:
(7*6)+(6*4)+(5*4)+(4*6)+(3*2)+(2*0)+(1*0)=116
116 % 10 = 6
So 64462-00-6 is a valid CAS Registry Number.

64462-00-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name pentadec-2-enal

1.2 Other means of identification

Product number -
Other names 2-Pentadecenal

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:64462-00-6 SDS

64462-00-6Downstream Products

64462-00-6Relevant academic research and scientific papers

AN EFFICIENT REAGENT FOR SYNTHESIS OF α,β-UNSATURATED ALDEHYDES 3-METHYLTHIO-2-PROPENYL p-TOLYL SULFONE

Ogura, Katsuyuki,Iihama, Teruyuki,Takahashi, Kazumasa,Iida, Hirodata

, p. 2671 - 2674 (2007/10/02)

Alkylation of 3-methylthio-2-propenyl p-tolyl sulfone (1) with an alkyl halide and a base (NaH or KOH-TOMAC) took place at the position α to the sulfonyl group to give optionally a mono- or dialkylated product (2 or 3), which was converted to β-monosubstituted or β,β-disubstituted α,β-unsaturated aldehyde (6 or 7), respectively, by TiCl4-assisted hydrolysis followed by the removal of p-toluenesulfinic acid.

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