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1,5-dimethyl-1-vinylhex-4-enyl pivalate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

83846-55-3

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83846-55-3 Usage

Physical state

Colorless to pale yellow liquid

Aroma

Fruity

Usage

Flavoring agent in food and beverage industry

Natural occurrence

Found in fruits like apples and blueberries

Additional uses

Production of perfumes and cosmetics

Safety

Generally recognized as safe (GRAS) by the FDA

Application

Used as a fragrance ingredient in personal care products and household items

Check Digit Verification of cas no

The CAS Registry Mumber 83846-55-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,8,4 and 6 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 83846-55:
(7*8)+(6*3)+(5*8)+(4*4)+(3*6)+(2*5)+(1*5)=163
163 % 10 = 3
So 83846-55-3 is a valid CAS Registry Number.
InChI:InChI=1/C15H26O2/c1-8-15(7,11-9-10-12(2)3)17-13(16)14(4,5)6/h8,10H,1,9,11H2,2-7H3

83846-55-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,7-dimethylocta-1,6-dien-3-yl 2,2-dimethylpropanoate

1.2 Other means of identification

Product number -
Other names EINECS 281-031-9

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:83846-55-3 SDS

83846-55-3Downstream Products

83846-55-3Relevant academic research and scientific papers

Dendronized cyclocopolymers with a radial gradient of polarity and their use to catalyze a difficult esterification

Liang, Catherine O.,Helms, Brett,Hawker, Craig J.,Frechet, Jean M. J.

, p. 2524 - 2525 (2003)

A cyclocopolymer containing pyrrolidinopyridine pendant groups was dendronized with polyester dendrons terminated with long alkyl chain ends and the microenvironment created by the dendrons was used to catalyze the difficult esterification of a tertiary alcohol with pivalic anhydride.

Effects of polymer architecture and nanoenvironment in acylation reactions employing dendritic (Dialkylamino)pyridine catalysts

Helms, Brett,Liang, Catherine O.,Hawker, Craig J.,Frechet, Jean M. J.

, p. 5411 - 5415 (2008/02/01)

The role of architecture and nanoenvironment in the catalytic properties of dendritic polymers containing 4-(dialkylamino)pyridines was investigated in the context of acylation reactions employing sterically demanding tertiary alcohols as substrates. Frechet-type benzyl ether and aliphatic ester dendrimers were prepared in a convergent manner from a common trivalent core containing three DMAP groups while a linear polymer was dendronized with aliphatic esters using a divergent growth scheme. Catalysis experiments clearly indicate that nanoenvironment plays the dominant role in determining the activity of the polymer catalysts, with the polyester platform being superior to the benzyl ether. Polymer architecture played little or no role in affecting catalysis. With respect to molecular transport and catalysis, this represents the first comparative study of the effect of architecture and nanoenvironment using structurally similar dendritic materials.

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