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58475-04-0

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58475-04-0 Usage

Chemical Properties

Clear colorless liquid; floral-like odor

Check Digit Verification of cas no

The CAS Registry Mumber 58475-04-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,4,7 and 5 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 58475-04:
(7*5)+(6*8)+(5*4)+(4*7)+(3*5)+(2*0)+(1*4)=150
150 % 10 = 0
So 58475-04-0 is a valid CAS Registry Number.
InChI:InChI=1/C10H20O/c1-3-5-7-10(4-2)8-6-9-11/h9-10H,3-8H2,1-2H3

58475-04-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-ethyloctanal

1.2 Other means of identification

Product number -
Other names 4-ethyl-octanal

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:58475-04-0 SDS

58475-04-0Synthetic route

4-ethyl-octan-1-ol
38514-07-7

4-ethyl-octan-1-ol

4-ethyl-octanal
58475-04-0

4-ethyl-octanal

58475-04-0Upstream product

58475-04-0Downstream Products

58475-04-0Relevant articles and documents

Comprehensive screening of octopus amphiphiles as DNA activators in lipid bilayers: Implications on transport, sensing and cellular uptake

Montenegro, Javier,Fin, Andrea,Matile, Stefan

supporting information; experimental part, p. 2641 - 2647 (2011/05/15)

Dynamic octopus amphiphiles contain one charged "head," here a guanidinium cation, together several hydrophobic "tails" (or "tentacles") that can be attached and exchanged in situ by reversible hydrazone formation. Quite surprisingly, their ability to activate DNA as transporters in lipid bilayer membranes was found to increase with the number of tails (up to four) as well as with their length (up to eight carbons). Both encouraged and puzzled by these results, we decided that a comprehensive screening of octopus amphiphiles with regard to number (from one to six) and length (from three to eighteen carbons) of their tails would be appropriate at this point. For this purpose, we here report the synthesis of cationic hexahydrazide peptide dendrons together with that of aldehydes with long, saturated, unsaturated and branched hydrophobic tails. Comprehensive screening of the completed collection of tails and heads reveals that the ability of octopus amphiphiles to activate DNA transporters shifts with increasing number of tails to decreasing length of the tails. Moreover, cis-alkenyl and branched alkyl tails are more active than their linear analogs, branched aromatic tails are best. These overall very meaningful trends for octopus amphiphiles will be of importance for sensing applications and fragrant cellular uptake.

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