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6289-70-9

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6289-70-9 Usage

General Description

"(2E)-2-(phenylmethylidene)decanal" is a chemical compound with the molecular formula C17H26O. It is a long-chain aldehyde with a phenyl group and a double bond, creating a linear carbon chain. (2E)-2-(phenylmethylidene)decanal is commonly used in the fragrance industry due to its pleasant odor and is often found in perfumes, colognes, and other scented products. It also has potential applications in the pharmaceutical and cosmetic industries. Additionally, this compound has been studied for its potential antimicrobial and antioxidant properties, making it a subject of interest in the field of natural product chemistry and biotechnology. Overall, "(2E)-2-(phenylmethylidene)decanal" is a versatile chemical with various industrial and biological applications.

Check Digit Verification of cas no

The CAS Registry Mumber 6289-70-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,8 and 9 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6289-70:
(6*6)+(5*2)+(4*8)+(3*9)+(2*7)+(1*0)=119
119 % 10 = 9
So 6289-70-9 is a valid CAS Registry Number.

6289-70-9SDS

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 (2E)-2-benzylidenedecanal

1.2 Other means of identification

Product number -
Other names -

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:6289-70-9 SDS

6289-70-9Downstream Products

6289-70-9Relevant articles and documents

Direct β-C(sp3)-H Functionalization of Aliphatic Amines to α,β-Unsaturated Imines, Aldehydes, and Chromenes

Mandal, Sumana,Mahato, Sujit,Jana, Chandan K.

supporting information, p. 3762 - 3765 (2015/08/18)

A metal-free method for direct β-C(sp3)-H functionalization of aliphatic amine was developed. The method is based on a reaction that yields enamine directly from the corresponding aliphatic amine, which otherwise requires the aid of metallic reagent and/or external oxidant. The reaction is operationally simple, general, and highly efficient in functionalizing both cyclic and acyclic amines. Structurally diverse unsaturated imines were obtained from N-heterocycles, while acyclic amines provided 2-alkyl cinnamaldehyde and benzopyran derivatives with excellent E/Z-selectivity.

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