4798-46-3

Basic information

• Product Name: 1-Hexen-3-ol, 5-methyl-
• CAS NO: 4798-46-3
• Molecular Formula: C7H14O
• Molecular Weight: 114.188
• Mol File: 4798-46-3.mol
• Article Data: 22

Chemical Properties

• CAS DataBase Reference: 1-Hexen-3-ol, 5-methyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Hexen-3-ol, 5-methyl-(4798-46-3)
• EPA Substance Registry System: 1-Hexen-3-ol, 5-methyl-(4798-46-3)

Safety Data

• Hazardous Substances Data: 4798-46-3(Hazardous Substances Data)

Usage

General Description

1-Hexen-3-ol, 5-methyl- is a chemical compound belonging to the family of hexenols. It is also known by its systematic name, 5-methyl-1-hexen-3-ol. This colorless liquid is a fragrance ingredient with a green, grassy odor reminiscent of freshly cut green leaves. It is used in the formulation of perfumes and other cosmetics due to its pleasant scent. Additionally, it is used as a flavoring agent in the food industry, particularly in baked goods and beverages. Its chemical structure includes a six-carbon chain with a double bond and a hydroxyl group, making it an unsaturated alcohol. 1-Hexen-3-ol, 5-methyl- is considered to have low toxicity and is generally regarded as safe for use in consumer products.

Upstream product

• 107-02-8 acrolein 
• 590-86-3 isovaleraldehyde 
• 1826-67-1 vinyl magnesium bromide 
• 920-36-5 (2-methylpropyl)lithium 
• 78-77-3 Isobutyl bromide 
• 91525-78-9 Diethoxy-methyl-(3-methyl-1-vinyl-butyl)-silane 
• 926-62-5 isobutylmagnesium bromide 
• 5674-02-2 2-methylpropylmagnesium chloride 
• 3536-96-7 vinylmagnesium chloride 

Downstream Products

• 623-56-3 5-methyl-3-hexanone 
• 591-76-4 2-Methylhexane 
• 2892-18-4 5-methyl-1-phenyl-hex-1-en-3-one 
• 1443776-16-6 C₁₈H₂₅NO₄S 
• 1443776-12-2 C₁₈H₂₇NO₅S 
• 1404461-26-2 C₁₅H₂₃NO 
• 49642-07-1 statine 
• 142810-26-2 (2R,3R)-1,2-epoxy-5-methyl-3-(4'-nitrobenzoyl)hexane 
• 142810-27-3 (2S,3S)-1,2-epoxy-5-methyl-3-(4'-nitrobenzoyl)hexane 
• 196706-15-7 (E)-(S)-2-Benzyl-7-methyl-oct-4-enoic acid ((1S,2S)-2-hydroxy-1-methyl-2-phenyl-ethyl)-methyl-amide 
• 196706-11-3 (E)-(S)-2-Benzyl-7-methyl-oct-4-enoic acid ((1R,2R)-2-hydroxy-1-methyl-2-phenyl-ethyl)-methyl-amide 
• 196706-10-2 (E)-7-Methyl-oct-4-enoic acid ((1R,2R)-2-hydroxy-1-methyl-2-phenyl-ethyl)-methyl-amide 

Relevant articles and documents

AN ENANTIOSPECIFIC AND VERSATILE SYNTHESIS OF STATINE

A short, enantiospecific synthesis of statine is described, starting from a readily available aldehyde.The control of chirality was effected by using the Sharpless asymmetric epoxidation procedure.

Enantio- And Diastereoselective Construction of Contiguous Tetrasubstituted Chiral Carbons in Organocatalytic Oxadecalin Synthesis

The organocatalytic enantio- and diastereoselective cycloetherification of 1,3-cyclohexanedione-bearing enones involving the in situ generation of chiral cyanohydrins was developed. This transformation offers the first catalytic asymmetric approach to oxa

Hydroxymethylation beyond Carbonylation: Enantioselective Iridium-Catalyzed Reductive Coupling of Formaldehyde with Allylic Acetates via Enantiotopic π-Facial Discrimination

Chiral iridium complexes modified by SEGPHOS catalyze the 2-propanol-mediated reductive coupling of branched allylic acetates 1a-1o with formaldehyde to form primary homoallylic alcohols 2a-2o with excellent control of regio- and enantioselectivity. These