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2,2,4-Trimethyl-4-penten-1-ol, also known as prenol or isoamyl vinyl carbinol, is a colorless liquid organic compound with the chemical formula C8H16O. It is an alcohol with a molecular weight of 128.21 g/mol. 2,2,4-Trimethyl-4-penten-1-ol is characterized by its unique structure, featuring a pentenyl chain with three methyl groups attached to the second and fourth carbon atoms, and a hydroxyl group at the first carbon. It is commonly used as a solvent, a reagent in organic synthesis, and a precursor in the production of various chemicals, such as perfumes and flavorings. Due to its reactive nature, it is also used in the synthesis of isoprenoids, which are important in the biosynthesis of natural products like vitamins, hormones, and essential oils.

53907-70-3

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53907-70-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53907-70-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,9,0 and 7 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 53907-70:
(7*5)+(6*3)+(5*9)+(4*0)+(3*7)+(2*7)+(1*0)=133
133 % 10 = 3
So 53907-70-3 is a valid CAS Registry Number.

53907-70-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2,4-trimethyl-pent-4-en-1-ol

1.2 Other means of identification

Product number -
Other names 2,2,4-Trimethyl-pent-4-en-1-ol

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:53907-70-3 SDS

53907-70-3Relevant academic research and scientific papers

Rhodium-Catalyzed Cyclization of O,ω-Unsaturated Alkoxyamines: Formation of Oxygen-Containing Heterocycles

Escudero, Julien,Bellosta, Véronique,Cossy, Janine

supporting information, p. 574 - 578 (2018/02/21)

O,ω-Unsaturated N-tosyl alkoxyamines undergo unexpected RhIII-catalyzed intramolecular cyclization by oxyamination to produce oxygen-containing heterocycles. Mechanistic studies show that an aziridine intermediate seems to be responsible for the formation of the heterocycles, possibly via a RhV species.

FUSED FURAN CONSTRUCTION VIA AN INTRAMOLECULAR CYCLOADDITION REACTION: SYNTHESES OF 4H-CYCLOHEPTA- AND 4H-CYCLOPENTAFURANS

Shishido, Kozo,Umimoto, Koji,Shibuya, Masayuki

, p. 641 - 658 (2007/10/02)

General and efficient syntheses of 4H-cyclohepta- and 4H-cyclopentafurans (4 and 5) have been accomplished employing the intramolecular dipolar cycloaddition based fused furan construction strategy.Treatment of the oximes (20 and 29), readily pre

Intramolecular Olefinic Aldehyde Prins Reactions for the Construction of Five-Membered Rings

Andersen, Niels H.,Hadley, Stephen W.,Kelly, James D.,Bacon, E. R.

, p. 4144 - 4151 (2007/10/02)

Four catalysts (Me2AlCl SnCl4 > EtAlCl2 > Et2AlCl) for the cyclization of olefinic aldehydes by an internal Prins mechanism have been compared by using systems that afford five-membered rings by type I and type II ene processes.Stannic chloride and Me

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