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4-METHYL-1-PENTEN-3-OL, also known as 4-Methyl-1-penten-3-ol, is a chemical compound with the molecular formula C6H12O. It is classified as an alcohol, containing a hydroxyl functional group attached to a 4-carbon chain with a methyl substituent on the first carbon. This colorless liquid has a strong odor and is flammable, necessitating careful handling and storage.

4798-45-2

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4798-45-2 Usage

Uses

Used in Fragrance Industry:
4-METHYL-1-PENTEN-3-OL is used as a flavoring agent for its sweet, fruity aroma, making it a popular choice in the fragrance industry.
Used in Chemical Production:
4-METHYL-1-PENTEN-3-OL is used as an intermediate in the production of other chemicals and pharmaceuticals, contributing to the synthesis of various compounds for different applications.

Check Digit Verification of cas no

The CAS Registry Mumber 4798-45-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,7,9 and 8 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4798-45:
(6*4)+(5*7)+(4*9)+(3*8)+(2*4)+(1*5)=132
132 % 10 = 2
So 4798-45-2 is a valid CAS Registry Number.
InChI:InChI=1/C6H12O/c1-4-6(7)5(2)3/h4-7H,1H2,2-3H3

4798-45-2SDS

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 4-methylpent-1-en-3-ol

1.2 Other means of identification

Product number -
Other names 3-hydroxy-4-methyl-1-pentene

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:4798-45-2 SDS

4798-45-2Relevant academic research and scientific papers

The reactivity of epoxides with lithium 2,2,6,6-tetramethylpiperidide in combination with organolithiums or grignard reagents

Hodgson, David M.,Fleming, Matthew J.,Stanway, Steven J.

, p. 4763 - 4773 (2008/02/04)

(Chemical Equation Presented) The scope and limitations of lithium 2,2,6,6-tetramethylpiperidide (LTMP)-modified reductive alkylation of epoxides is detailed. A variety of organolithiums are added to terminal and 2,2-disubstituted epoxides in the presence of LTMP to generate alkenes in a completely regio- and highly stereoselective manner. Arylated alkenes, dienes, allylsilanes, and enynes are accessed using this procedure. The methodology is applied in the synthesis of the roller leaf moth pheromone, (3E,5Z)-dodecadienyl acetate. The corresponding reaction without LTMP has also been examined, and a study using deuterated epoxides provides insight into the mechanism. In the presence of LTMP, Grignard reagents are also shown to produce E-alkenes directly from epoxides.

Cyclodehydration of some 1,n-diols catalysed by sulfated zirconia

Wali, Anil,Pillai, S. Muthukumaru

, p. 326 - 327 (2007/10/03)

Sulfated zirconia, a solid acid is found to be a good catalyst in the cyclodehydration of several diols.

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