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Heptanoic acid, 2-ethenyl-, also known as 2-vinylheptanoic acid, is a colorless liquid organic compound with the chemical formula C9H16O2. It is a derivative of heptanoic acid, featuring a vinyl group (C2H3) attached to the second carbon atom of the heptanoic acid chain. This unsaturated fatty acid is characterized by its molecular weight of 156.22 g/mol and a density of approximately 0.93 g/cm3. It is insoluble in water but soluble in organic solvents such as ethanol and ether. 2-Ethenylheptanoic acid is primarily used in the synthesis of various chemicals, pharmaceuticals, and as a building block in the production of specialty polymers. It is also found in trace amounts in some natural products, such as certain essential oils and plant extracts.

4436-85-5

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4436-85-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4436-85-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,3 and 6 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4436-85:
(6*4)+(5*4)+(4*3)+(3*6)+(2*8)+(1*5)=95
95 % 10 = 5
So 4436-85-5 is a valid CAS Registry Number.

4436-85-5SDS

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 2-vinylheptanoic acid

1.2 Other means of identification

Product number -
Other names 2-Vinyl-heptanoic acid

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:4436-85-5 SDS

4436-85-5Downstream Products

4436-85-5Relevant academic research and scientific papers

Switchable Site-Selective Catalytic Carboxylation of Allylic Alcohols with CO2

van Gemmeren, Manuel,B?rjesson, Marino,Tortajada, Andreu,Sun, Shang-Zheng,Okura, Keisho,Martin, Ruben

supporting information, p. 6558 - 6562 (2017/05/29)

A switchable site-selective catalytic carboxylation of allylic alcohols has been developed in which CO2 is used with dual roles, both facilitating C?OH cleavage and as a C1 source. This protocol is characterized by its mild reaction conditions, absence of stoichiometric amounts of organometallic reagents, broad scope, and exquisite regiodivergency which can be modulated by the type of ligand employed.

Ligand-controlled regiodivergent Ni-catalyzed reductive carboxylation of allyl esters with CO2

Moragas, Toni,Cornella, Josep,Martin, Ruben

, p. 17702 - 17705 (2015/02/19)

A novel Ni-catalyzed regiodivergent reductive carboxylation of allyl esters with CO2 has been developed. This mild, user-friendly, and operationally simple method is characterized by an exquisite selectivity profile that is dictated by the ligand backbone.

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