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2-[(2-Pentylcyclopropyl)methyl]cyclopropaneoctanoic acid methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

56687-67-3

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56687-67-3 Usage

Molecular structure

A complex structure derived from cyclopropane and octanoic acid.

Cyclopropane ring

Contains a ring with three carbon atoms.

Substitution

The cyclopropane ring is substituted with a pentylcyclopropylmethyl group.

Octanoic acid portion

A part of the molecule consisting of an eight-carbon chain with a carboxylic acid group.

Esterification

The octanoic acid portion is esterified with a methyl group.

Unique properties

Possesses potential unique physical and chemical properties due to its intricate structure.

Potential applications

May have uses in organic synthesis or pharmaceutical research.

Further research

Requires additional studies and analysis to fully understand its characteristics and potential uses.

Check Digit Verification of cas no

The CAS Registry Mumber 56687-67-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,6,8 and 7 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 56687-67:
(7*5)+(6*6)+(5*6)+(4*8)+(3*7)+(2*6)+(1*7)=173
173 % 10 = 3
So 56687-67-3 is a valid CAS Registry Number.

56687-67-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name DCPLA methyl ester

1.2 Other means of identification

Product number -
Other names 8-[2-(2-pentylcyclopropylmethyl)cyclopropyl]octanoic acid methyl ester

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:56687-67-3 SDS

56687-67-3Downstream Products

56687-67-3Relevant academic research and scientific papers

PKC activators and combinations thereof

-

Page/Page column 44, (2020/11/13)

The present disclosure relates to PKC activators and combinations thereof. The disclosure further relates to compositions, kits, uses, and methods thereof.

Design and synthesis of protein kinase C epsilon selective diacylglycerol lactones (DAG-lactones)

Ann, Jihyae,Yoon, Suyoung,Baek, Jisoo,Kim, Da Hye,Lewin, Nancy E.,Hill, Colin S.,Blumberg, Peter M.,Lee, Jeewoo

, p. 332 - 341 (2015/05/04)

DAG-lactones afford a synthetically accessible, high affinity platform for probing structure activity relationships at the C1 regulatory domain of protein kinase C (PKC). Given the central role of PKC isoforms in cellular signaling, along with their differential biological activities, a critical objective is the design of isoform selective ligands. Here, we report the synthesis of a series of DAG-lactones varying in their side chains, with a particular focus on linoleic acid derivatives. We evaluated their selectivity for PKC epsilon versus PKC alpha both under standard lipid conditions (100% phosphatidylserine, PS) as well as in the presence of a nuclear membrane mimetic lipid mixture (NML). We find that selectivity for PKC epsilon versus PKC alpha tended to be enhanced in the presence of the nuclear membrane mimetic lipid mixture and, for our lead compound, report a selectivity of 32-fold.

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