Welcome to LookChem.com Sign In|Join Free
  • or
Longiborneol is a naturally occurring sesquiterpene alcohol, characterized by its molecular formula C15H26O. It is derived from the longifolene, a bicyclic sesquiterpene hydrocarbon, and is found in various plant species, including Juniperus longifolia and some species of the genus Pogostemon. Longiborneol exhibits a wide range of biological activities, such as anti-inflammatory, antimicrobial, and antioxidant properties. It is also used in the fragrance industry due to its pleasant scent and is a potential candidate for pharmaceutical applications, particularly in the development of new drugs targeting various diseases.

465-24-7

Post Buying Request

465-24-7 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

465-24-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 465-24-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,6 and 5 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 465-24:
(5*4)+(4*6)+(3*5)+(2*2)+(1*4)=67
67 % 10 = 7
So 465-24-7 is a valid CAS Registry Number.

465-24-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,4-methanoazulen-9-ol, decahydro-1,5,5,8α-tetramethyl-(1R,3αR,4S,8αS,9S)-

1.2 Other means of identification

Product number -
Other names (+)-Longiborneol

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:465-24-7 SDS

465-24-7Relevant academic research and scientific papers

Enanthiospecific synthesis of longiborneol and longifolene

Kuo, David L.,Money, Thomas

, p. 1794 - 1804 (2007/10/02)

A trimethylsilyl enol ether (34) derived from camphor (1) undergoes intramolecular Mukaiyama reaction to provide a tricyclic ketone (36) that can serve as a key intermediate in a new enantiospecific synthesis of longiborneol (11) and longifolene (12).

An Enantiospecific Synthesis of Longiborneol and Longifolene

Kuo, David L.,Money, Thomas

, p. 1691 - 1692 (2007/10/02)

(+)-8-Bromocamphor (7) is readily converted into a chiral enol ether acetal (8) which undergoes TiCl4-promoted cyclization to provide a tricyclic intermediate that can serve as a synthetic precursor of longibornane and longifolane sesquiterpenoids.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 465-24-7