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3-Methyl-2-pentenal is an organic compound with the molecular formula C6H10O. It is a colorless liquid with a strong, pungent odor and is classified as an aldehyde. This chemical is an important intermediate in the synthesis of various fragrances, flavors, and pharmaceuticals due to its unique reactivity and functional group. It is commonly used in the production of ionones, which are key components in the creation of rose-like scents, as well as in the synthesis of vitamins and other specialty chemicals. 3-Methyl-2-pentenal is also known for its ability to react with amines to form Schiff bases, which are useful in the preparation of various pharmaceuticals and agrochemicals. Its industrial applications are vast, and it is a key building block in the chemical industry.

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  • 3592-19-6 Structure
  • Basic information

    1. Product Name: 3-Methyl-2-pentenal
    2. Synonyms: 3-Methyl-2-pentenal
    3. CAS NO:3592-19-6
    4. Molecular Formula: C6H10O
    5. Molecular Weight: 98.143
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 3592-19-6.mol
  • Chemical Properties

    1. Melting Point: -78°C (estimate)
    2. Boiling Point: 133.68°C (estimate)
    3. Flash Point: 33.4°C
    4. Appearance: /
    5. Density: 0.8483 (estimate)
    6. Vapor Pressure: 7.34mmHg at 25°C
    7. Refractive Index: 1.4276 (estimate)
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 3-Methyl-2-pentenal(CAS DataBase Reference)
    11. NIST Chemistry Reference: 3-Methyl-2-pentenal(3592-19-6)
    12. EPA Substance Registry System: 3-Methyl-2-pentenal(3592-19-6)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 3592-19-6(Hazardous Substances Data)

3592-19-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3592-19-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,9 and 2 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 3592-19:
(6*3)+(5*5)+(4*9)+(3*2)+(2*1)+(1*9)=96
96 % 10 = 6
So 3592-19-6 is a valid CAS Registry Number.
InChI:InChI=1/C6H10O/c1-3-6(2)4-5-7/h4-5H,3H2,1-2H3

3592-19-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (Z)-3-methylpent-2-enal

1.2 Other means of identification

Product number -
Other names -

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:3592-19-6 SDS

3592-19-6Downstream Products

3592-19-6Relevant articles and documents

3 - Methyl pentyl acetate and flavoring agent -3 - mercapto

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Paragraph 0061; 0066-0067, (2021/04/16)

To provide a novel flavoring agent.SOLUTION: Provided are a flavor improvement method of a perfume of a perfume composition comprising: a step of providing a flavoring agent comprising 3-mercapto-3-methyl pentyl acetate represented by the following formula (1), a flavoring agent containing it as an active ingredient, and a consumer goods containing the flavoring agent or the perfume composition; and, furthermore a step of blending the flavoring agent made of 3-mercapto-3-methyl pentyl acetate represented by the following formula (1) to the perfume composition, and a method of improving the perfume of the consumer goods comprising blending the flavoring agent or the perfume composition to the consumer goods.SELECTED DRAWING: None

SULFUR-CONTAINING COMPOUND AND FLAVORING AGENT

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Paragraph 0085; 0088, (2021/09/27)

PROBLEM TO BE SOLVED: To provide a novel sulfur-containing compound and a flavoring agent, a perfume composition and consumer goods, a method for improving flavor of the perfume composition, and a method for improving flavor of the consumer goods.SOLUTION: This invention provides: a sulfur-containing compound expressed by Formula (1); a flavoring agent comprising the compound expressed by Formula (1); a perfume composition containing the sulfur-containing compound or the flavoring agent; consumer goods containing the sulfur-containing compound, the flavoring agent or the perfume composition; a method for improving flavor of the perfume composition including a step of mixing the sulfur-containing compound or the flavoring agent into the perfume composition; and a method for improving flavor of the consumer goods including a step of mixing the sulfur-containing compound, the flavoring agent or the perfume composition into the consumer goods.SELECTED DRAWING: NoneCOPYRIGHT: (C)2021,JPOandINPIT

DIHYDROOROTATE DEHYDROGENASE INHIBITORS

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Page/Page column 75; 85, (2020/10/28)

Disclosed are compounds, compositions and methods for treating diseases, disorders, or medical conditions that are affected by the modulation of DHODH. Such compounds are represented by Formula (I) as follows: wherein R1, R2, R3, R4, X, and Y are defined herein.

DIHYDROOROTATE DEHYDROGENASE INHIBITORS

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Page/Page column 59; 153-155, (2020/08/22)

Disclosed are compounds, compositions and methods for treating diseases, disorders, or medical conditions that are affected by the modulation of DHODH. Embodiments of such compounds are represented by Formula (I) as follows: 5 wherein R1, R2, R3, R4, R5a, R5b, X and Y, are defined herein.

Cis-dioxomolybdenum(VI) complexes as new catalysts for the Meyer-Schuster rearrangement

Lorber, Christian Y.,Osborn, John A.

, p. 853 - 856 (2007/10/03)

We describe a new catalytic system for the isomerisation of propargylic alcohols into α,β-ethylenic carbonyl derivatives (Meyer-Schuster rearrangement), based on the combination of dioxomolybdenum(IV) catalysts and sulfoxides.

CONVERSION OF α ACETYLENIC ALCOHOLS INTO αβ UNSATURATED ALDEHYDES

Julia, Marc,Lefebvre, Christian

, p. 189 - 192 (2007/10/02)

Very mild conditions have been found for the efficient regioselective addition of phenylthiol to ethynyl carbinols.A biphasic aqueous acid hydrolysis then leads to αβ-unsaturated aldehydes.The Meyer-Schuster rearrangement is thus brought about in two steps.

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