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101409-58-9

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101409-58-9 Usage

General Description

(10S)-12-Methoxy-9,10-seco-9,20-cycloabieta-8,11,13-triene-10,11-diol is a complex chemical compound that is derived from the sesquiterpene class of natural products. It contains a cycloabieta-8,11,13-triene backbone with a methoxy group at the 12th position, and hydroxyl groups at the 10th and 11th positions. (10S)-12-Methoxy-9,10-seco-9,20-cycloabieta-8,11,13-triene-10,11-diol has potential biological and pharmacological activities, and it may be used in various medicinal and therapeutic applications. However, further research is needed to fully understand its properties and potential uses.

Check Digit Verification of cas no

The CAS Registry Mumber 101409-58-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,4,0 and 9 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 101409-58:
(8*1)+(7*0)+(6*1)+(5*4)+(4*0)+(3*9)+(2*5)+(1*8)=79
79 % 10 = 9
So 101409-58-9 is a valid CAS Registry Number.

101409-58-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name salvicanol

1.2 Other means of identification

Product number -
Other names (5aS,9aS)-2-Isopropyl-3-methoxy-9,9-dimethyl-5,6,7,8,9,9a,10,11-octahydro-dibenzo[a,d]cycloheptene-4,5a-diol

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:101409-58-9 SDS

101409-58-9Downstream Products

101409-58-9Relevant articles and documents

Collective Syntheses of Icetexane Natural Products Based on Biogenetic Hypotheses

Thommen, Christophe,Neuburger, Markus,Gademann, Karl

, p. 120 - 127 (2017)

A divergent synthesis of 10 icetexane natural products based on a proposed biogenetic cationic ring expansion of a reduced carnosic acid derivative is described. Of these icetexanes, (+)-salvicanol, (?)-cyclocoulterone, (?)-coulterone, (?)-obtusinone D, and (?)-obtusinone E have been synthesized for the first time. In addition, the hypothesis for the non-enzymatic biogenesis of benzo[1,3]dioxole natural products has been experimentally investigated. Additional experimental evidence for the abiotic formation of the methylenedioxy unit is provided, as photolysis of the quinone (+)-komaroviquinone resulted in the formation of the [1,3]dioxole-containing natural product (?)-cyclocoulterone and (+)-komarovispirone.

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