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(2E)-4-methylidenetetradec-2-enal is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

85769-28-4

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85769-28-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 85769-28-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,7,6 and 9 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 85769-28:
(7*8)+(6*5)+(5*7)+(4*6)+(3*9)+(2*2)+(1*8)=184
184 % 10 = 4
So 85769-28-4 is a valid CAS Registry Number.

85769-28-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (E)-4-methylidenetetradec-2-enal

1.2 Other means of identification

Product number -
Other names 2-Tetradecenal,4-methylene-,(2E)

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:85769-28-4 SDS

85769-28-4Downstream Products

85769-28-4Relevant academic research and scientific papers

Catalytic Regioselective γ-Methylenation of α,β-Unsaturated Aldehydes Using Formaldehyde via Vinylogous Aldol Condensation

Kutwal, Mahesh S.,Dev, Sachin,Appayee, Chandrakumar

, p. 2509 - 2513 (2019/04/30)

The first vinylogous aldol condensation of α,β-unsaturated aldehydes using aqueous formaldehyde is developed under mild reaction conditions to form the γ-methylenated products with excellent regioselectivity. Using this methodology, a short synthesis of α-triticene, an antifungal compound, is achieved in two steps. The practicality of this methodology is demonstrated by the gram-scale synthesis. Formation of the unusual double γ-functionalized products from crotonaldehyde and a direct asymmetric vinylogous aldol product from phenylglyoxal is also described.

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