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4-Penten-1-ol, 2-ethenyl-, also known as 2-Ethyl-4-penten-1-ol or 2-Ethyl-4-pentenol, is an organic compound with the chemical formula C7H14O. It is a colorless liquid with a strong, pungent odor. This unsaturated alcohol is characterized by the presence of a double bond between the second and third carbon atoms, as well as a hydroxyl group attached to the first carbon atom. 4-Penten-1-ol, 2-ethenyl- is used as a fragrance ingredient and a chemical intermediate in the synthesis of various compounds, including pharmaceuticals and agrochemicals. It is also found in trace amounts in some natural products, such as essential oils and plant extracts. Due to its reactive nature, it is important to handle 4-Penten-1-ol, 2-ethenyl- with care, as it can be irritating to the skin, eyes, and respiratory system.

5903-36-6

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5903-36-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5903-36-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,9,0 and 3 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5903-36:
(6*5)+(5*9)+(4*0)+(3*3)+(2*3)+(1*6)=96
96 % 10 = 6
So 5903-36-6 is a valid CAS Registry Number.

5903-36-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (+/-)-2-ethenyl-4-penten-1-ol

1.2 Other means of identification

Product number -
Other names 2-vinyl-4-penten-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:5903-36-6 SDS

5903-36-6Relevant academic research and scientific papers

Syntheses with Organoboranes. XI. Allylboration of Vinylic Epoxides with Allylic Dialkylboranes

Zaidlewicz, Marek,Krzeminski, Marek P.

, p. 3897 - 3899 (2007/10/03)

equation presented Allylboration of representative vinylic epoxides with allyldiethylborane (1) and (2-cyclohexenyl)dicyclohexylborane (2) affords the corresponding 1,2- and 1,4-addition products. cis-1,2-Addition is favored in the reaction of 1 with 3,4-

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