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16326-86-6

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16326-86-6 Usage

Description

OCTA-2,4,6-TRIENAL, also known as Octa-2,4,6-trienal, is a chemical compound with the CAS number 16326-86-6. It is a yellow solid and is primarily used in organic synthesis due to its unique chemical properties.

Uses

Used in Organic Synthesis:
OCTA-2,4,6-TRIENAL is used as a synthetic building block for the creation of various organic compounds. Its chemical structure allows it to be a versatile component in the synthesis of different molecules, making it a valuable asset in the field of organic chemistry.
Used in Pharmaceutical Industry:
OCTA-2,4,6-TRIENAL is used as an intermediate in the development of pharmaceutical compounds. Its unique properties enable it to be a key component in the synthesis of drugs with specific therapeutic applications.
Used in Chemical Research:
OCTA-2,4,6-TRIENAL is used as a research tool in the study of chemical reactions and mechanisms. Its properties make it an interesting subject for understanding various aspects of organic chemistry and potentially discovering new reactions or applications.
Used in Material Science:
OCTA-2,4,6-TRIENAL can be used as a component in the development of new materials with specific properties. Its chemical structure may contribute to the creation of materials with unique characteristics, such as improved stability or reactivity.

Check Digit Verification of cas no

The CAS Registry Mumber 16326-86-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,3,2 and 6 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 16326-86:
(7*1)+(6*6)+(5*3)+(4*2)+(3*6)+(2*8)+(1*6)=106
106 % 10 = 6
So 16326-86-6 is a valid CAS Registry Number.

16326-86-6SDS

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 (2E,4E,6E)-2,4,6-Octatrienal

1.2 Other means of identification

Product number -
Other names retrofractamide B

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:16326-86-6 SDS

16326-86-6Relevant articles and documents

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Ogawa,M. et al.

, p. 3813 - 3817 (1973)

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Length-Selective Synthesis of Acylglycerol-Phosphates through Energy-Dissipative Cycling

Bonfio, Claudia,Caumes, Cécile,Duffy, Colm D.,Patel, Bhavesh H.,Percivalle, Claudia,Tsanakopoulou, Maria,Sutherland, John D.

supporting information, p. 3934 - 3939 (2019/03/08)

The main aim of origins of life research is to find a plausible sequence of transitions from prebiotic chemistry to nascent biology. In this context, understanding how and when phospholipid membranes appeared on early Earth is critical to elucidating the prebiotic pathways that led to the emergence of primitive cells. Here we show that exposing glycerol-2-phosphate to acylating agents leads to the formation of a library of acylglycerol-phosphates. Medium-chain acylglycerol-phosphates were found to self-assemble into vesicles stable across a wide range of conditions and capable of retaining mono- and oligonucleotides. Starting with a mixture of activated carboxylic acids of different lengths, iterative cycling of acylation and hydrolysis steps allowed for the selection of longer-chain acylglycerol-phosphates. Our results suggest that a selection pathway based on energy-dissipative cycling could have driven the selective synthesis of phospholipids on early Earth.

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