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1845-30-3

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1845-30-3 Usage

General Description

Cis-verbenol is a natural organic compound that is found in the essential oil of various plants, including cypress and pine. It is classified as a terpene alcohol and is known for its pleasant, woody, and slightly floral odor. Cis-verbenol is commonly used in the fragrance industry as a scent enhancer, and it is also of interest to the agricultural industry, as it serves as a pheromone precursor for certain bark beetle species. Additionally, it has been shown to possess antifungal and antibacterial properties, making it a potential candidate for use in natural pesticides and antimicrobial products.

Check Digit Verification of cas no

The CAS Registry Mumber 1845-30-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,4 and 5 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1845-30:
(6*1)+(5*8)+(4*4)+(3*5)+(2*3)+(1*0)=83
83 % 10 = 3
So 1845-30-3 is a valid CAS Registry Number.

1845-30-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (1S,2S,5S)-4,6,6-trimethylbicyclo[3.1.1]hept-3-en-2-ol

1.2 Other means of identification

Product number -
Other names Bicyclo[3.1.1]hept-3-en-2-ol, 4,6,6-trimethyl-, (1α,2β,5α)-

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:1845-30-3 SDS

1845-30-3Relevant articles and documents

Individual stereoisomers of verbenol and verbenone express bioactive features

Ivanov, Marija,Kovalenko, Vitaly,Svirid, Anastasia,Kosti?, Marina,Petrovi?, Jovana,Stojkovi?, Dejan

, (2021/12/13)

Naturally occurring terpene core compounds have been used extensively in both pharmaceutical and cosmetic industry. However, since chirality of these compounds has profound influence on the level of their bioactivity, the aim of the present study was to a

Stereospecific synthesis of S-(?)-trans-verbenol and its antipode by inversion of sterically hindered alcohols

Fang, Jia-Xing,Kong, Xiang-Bo,Liu, Fu,Zhang, Su-Fang,Zhang, Zhen

, (2020/12/15)

S-(?)-trans-Verbenol (1) and its antipode, R-(+)-trans-verbenol (1′) have been confirmed as the critical pheromone components of bark beetles. Synthesis of these two active secondary alcohols (1 and 1′) from commercially available starting materials S-α-pinene and R-α-pinene was reported. The key steps were mainly depended on the effective SN2 stereo-inversion of the hydroxy group of sterically hindered alcohols (3 and 3′), using Mitsunobu reaction or hydrolysis of mesylate ester, alternatively. Our results provide a new and stereo-selectivity way to obtain optically active insect pheromones.

A Cu-Doped ZIF-8 metal organic framework as a heterogeneous solid catalyst for aerobic oxidation of benzylic hydrocarbons

Nagarjun, Nagarathinam,Dhakshinamoorthy, Amarajothi

, p. 18702 - 18712 (2019/12/09)

Mixed-metal metal organic frameworks have received considerable attention in recent years and it has been shown that the activity of the parent metal organic framework (MOF) is often enhanced upon doping with external metal ions within the framework. In this context, Cu2+ ions with different loadings were incorporated within the ZIF-8 framework to obtain a series of Cu-doped ZIF-8 materials and their activity was examined in the aerobic oxidation of hydrocarbons. The as-synthesized Cu-doped solids were characterized by powder X-ray diffraction (XRD), ultraviolet diffuse reflectance spectroscopy (UV-DRS), scanning electron microscopy (SEM), Fourier Transform infrared (FT-IR), electron paramagnetic resonance (EPR) and inductively coupled plasma (ICP) analysis. The experimental results revealed that the activity of Cu-doped ZIF-8 is much higher than that of the parent ZIF-8 in all the tested substrates at 120 °C. Furthermore, the activity of the Cu-doped ZIF-8 with the highest Cu loading was eight fold higher than that of the parent ZIF-8 in the aerobic oxidation of cyclooctane (1) at 120 °C with more than 80% selectivity to the corresponding cyclooctanol/cyclooctanone (ol/one) mixture. Cu-doped ZIF-8 was reused two times with no significant drop in its activity under identical conditions. Furthermore, comparison of the two times reused solid with that of the fresh solid by powder XRD and SEM analysis revealed identical structural integrity and morphology, respectively during the oxidation reactions.

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