74410-10-9

Basic information

• Product Name: dillether
• Synonyms: dillether;anethofuran;(3S,3aS,7aR)-3,6-dimethyl-2,3,3a,4,5,7a-hexahydrobenzofuran
• CAS NO: 74410-10-9
• Molecular Formula: C₁₀H₁₆O
• Molecular Weight: 152.23
• Mol File: 74410-10-9.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 207°C at 760 mmHg
• Flash Point: 73.6°C
• Appearance: /
• Density: 0.933g/cm³
• Vapor Pressure: 0.331mmHg at 25°C
• Refractive Index: 1.471
• CAS DataBase Reference: dillether(CAS DataBase Reference)
• NIST Chemistry Reference: dillether(74410-10-9)
• EPA Substance Registry System: dillether(74410-10-9)

Safety Data

• Hazardous Substances Data: 74410-10-9(Hazardous Substances Data)

Usage

Description

Dillether, also known as dillapiole, is a natural organic compound found in dill weed oil. It is characterized by its herbal type medium strength odor, which is recommended to be smelled in a 10.00% solution or less. Dillether is derived from the dill weed, which is a popular herb used in cooking and has a variety of applications in different industries.

Uses

Used in Flavor and Fragrance Industry:
Dillether is used as a flavoring agent for its distinct herbal aroma. It is commonly used in the food and beverage industry to add a unique taste and scent to various products.
Used in Aromatherapy:
Dillether is used as an essential oil in aromatherapy for its calming and soothing properties. It is believed to help with relaxation and stress relief.
Used in Perfumery:
Dillether is used as a fragrance ingredient in the perfumery industry due to its pleasant and distinctive herbal scent.
Used in Cosmetics:
Dillether is used as a natural additive in the cosmetics industry, particularly in products that aim to provide a refreshing and invigorating experience for the user.
Used in Pharmaceutical Industry:
Dillether has potential applications in the pharmaceutical industry, as it may have therapeutic properties that can be utilized in the development of new drugs or treatments.

InChI:InChI=1/C10H16O/c1-7-3-4-9-8(2)6-11-10(9)5-7/h5,8-10H,3-4,6H2,1-2H3/t8-,9+,10+/m1/s1

Upstream product

• 37905-03-6 8-hydroxygeranyl acetate 
• 70238-37-8 (2'Z,6'E)-Essigsaeure-(8'-hydroxy-3',7'-dimethyl-2',6'-octadien-1'-yl)ester 
• 88717-91-3 1-O-methyl-10-hydroxynerol 
• 88717-90-2 1-O-methyl-10-hydroxygeraniol 
• 106-25-2 Nerol 
• 106-24-1 Geraniol 
• 2565-83-5 geraniol methyl ether 
• 141-12-8 neryl acetate 
• 105-87-3 3,7-dimethyl-2E,6-octadien-1-yl acetate 
• 37905-02-5 (2E,6E)-3,7-dimethyl-8-oxoocta-2,6-dien-1-yl acetate 
• 2565-83-5 (2Z)-1-methoxy-3,7-dimethylocta-2,6-diene 
• 94853-00-6 (2Z,6E)-3,7-dimethyl-8-oxoocta-2,6-dien-1-yl acetate 
• 139372-89-7 E,E-2-formyl-8-methoxy-6-methyl-2,6-octadiene 
• 139372-89-7 (2E,6Z)-8-Methoxy-2,6-dimethyl-octa-2,6-dienal 

Downstream Products

• 13834-09-8 (1RS,3RS,4RS,8SR)-3,9-epoxymenthane 
• 13834-09-8 (3R,3aR,6R,7aR)-3,6-Dimethyl-octahydro-benzofuran 
• 5113-94-0 (+)-(8S)-1,4-trans-p-Menthanol-9 
• 5113-94-0 (+)-(8S)-1,4-cis-p-Menthanol-9 
• 494-90-6 menthofuran 
• 13341-72-5 (+/-)-3,6-dimethyl-5,6,7,7a-tetrahydrobenzofuran-2(4H)-one 
• 79726-51-5 (3S,3aS,6S,7aS)-3,6-Dimethyl-hexahydro-benzofuran-2-one 
• 79726-51-5 (3R,3aS,6S,7aS)-3,6-Dimethyl-hexahydro-benzofuran-2-one 
• 676248-66-1 (1R,4S,8S)-3-oxo-p-menthan-9-oic acid 
• 79726-52-6 (1R,4S,8S)-3-oxo-p-menthan-9-oic acid methyl ester 

Relevant articles and documents

Chemical Tranformation of Terpenoids. V. Acidic Conversions of 10-Hydroxygeraniol and 10-Hydroxynerol Derivatives Leading to Cyclic Monoterpenoids

Acid treatment of 1-O-acetyl-10-hydroxygeraniol (5a), 1-O-methyl-10-hydroxygeraniol (5b), 1-O-acetyl-10-hydroxynerol (6a), and 1-O-methyl-10-hydroxynerol (6b) was investigated under various conditions.It was found that treatment of 5a and 6a with HCOOH gave menth-1-ene-8,9-diol (7), while treatment of 5a, 5b, 6a, or 6b with BF3-etherate in CH2Cl2 furnished two menthofuran-type compounds (9, 10) and two bicyclooct-2-ene derivatives (17, 24).Both 9 and 10 were successfully converted to menthofuran (16) and 17 was converted to a bicyclooctenone derivative (23) which was a key intermediate for a synthesis of juvabione (27).Keywords - geraniol; nerol; 10-hydroxygeraniol; 10-hydroxynerol; 10-hydroxygeraniol derivative; 10-hydroxynerol derivative; uroterpenol; menthofuran; bicyclooct-2-ene derivative