Welcome to LookChem.com Sign In|Join Free
  • or
Propanedioic acid, (1,2-dimethyl-2-propenyl)-, diethyl ester, also known as diethyl 1,2-dimethyl-2-propenyl malonate, is a chemical compound with the molecular formula C11H18O4. It is a colorless liquid with a fruity odor and is used as a flavoring agent in the food and beverage industry. This ester is synthesized by the reaction of diethyl malonate with 1,2-dimethyl-2-propenyl bromide, and it is characterized by its ability to impart a pleasant, fruity aroma to various products. The compound is also used in the synthesis of other organic compounds and as a chemical intermediate in the pharmaceutical and fragrance industries. Due to its potential for skin and eye irritation, it is important to handle this chemical with care and proper safety measures.

759-30-8

Post Buying Request

759-30-8 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

759-30-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 759-30-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,5 and 9 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 759-30:
(5*7)+(4*5)+(3*9)+(2*3)+(1*0)=88
88 % 10 = 8
So 759-30-8 is a valid CAS Registry Number.

759-30-8SDS

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 diethyl 2-(3-methylbut-3-en-2-yl)propanedioate

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:759-30-8 SDS

759-30-8Downstream Products

759-30-8Relevant academic research and scientific papers

Etude de l'allylation, catalysee par le nickel, d'enolates stables, par les ethers et les alcools allyliques

Alvarez, Eleuterio,Cuvigny, Therese,Julia, Marc

, p. 199 - 212 (2007/10/02)

The allylation of stable enolates derived from diethyl malonate and ethyl cyanoacetate by a variety of aliphatic or aromatic allylic ethers and by allylic alcohols, under nickel catalysis, was investigated.The influence of ligands, solvents and temperature was studied.

SUBSTITUTIONS CATALYSEES AU NICKEL D'ACETATES ET DE SULFONES ALLYLIQUES

Cuvigny, Therese,Julia, Marc

, p. 383 - 408 (2007/10/02)

The allylic substitution of stable enolates derived from diethyl malonate, ethyl cyanoacetate, ethyl benzylsulfonylacetate, bis(benzenesulfonyl)methane and sodium p-toluenesulfinate by a variety of allylic esters and sulfones has been investigated.Suitable ligands and reaction conditions have been found to ensure high yields, and in some cases considerable control of the regioselectivity of the reaction.

ETUDE DE LA REGIOSELECTIVITE DE LA SUBSTITUTION DES CARBANIONS PAR DES DERIVATIVES ALLIQUES CATALYSEE AU PALLADIUM. OBTENTION SELECTIVE DE COMPOSES A CARBONE QUATERNAIRE

Cuvigny, Therese,Julia, Marc,Rolando, C.

, p. 395 - 414 (2007/10/02)

The influence of the leaving groups, carbanions and ligands on ?-allylpalladium has been investigated in the substitution of primary or tertiary terpene derivatives.Conditions have been found under which the substitution takes place essentially at one or the other end of the allylic system.This provides a new and convenient way to obtain compounds with quaternary carbon atoms, which has been exemplified by the synthesis of 3,3-dimethyl-4-pentenenitrile.

ALKYLATIONS ALLYLIQUES CATALYSEES AU NICKEL

Cuvigny, Therese,Julia, Marc

, p. C21 - C24 (2007/10/02)

Stable enolates such as diethyl malonate enolate can be smoothly substituted by allylic acetates (or sulfones) in the presence of nickel complexes.Sulfinate ions convert allylic acetates into sulfones.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 759-30-8