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30543-91-0

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30543-91-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 30543-91-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,5,4 and 3 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 30543-91:
(7*3)+(6*0)+(5*5)+(4*4)+(3*3)+(2*9)+(1*1)=90
90 % 10 = 0
So 30543-91-0 is a valid CAS Registry Number.

30543-91-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name sesquichamenol

1.2 Other means of identification

Product number -
Other names litseachromolaevane A

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:30543-91-0 SDS

30543-91-0Downstream Products

30543-91-0Relevant articles and documents

The first total syntheses of the sesquiterpenes (±)-1,10;7,10- bisepoxy-1,10-seco-calamanene and (±)-6,7;7,10-bisepoxy-6,7-seco- calamanene

Srikrishna,Ravi,Krishnan, Hema S.

scheme or table, p. 1199 - 1201 (2009/04/05)

First total syntheses of the tricyclic sesquiterpenes mentioned in the title containing a benzo-fused 2,8-dioxabicyclo[3.2.1]octane framework, confirming the structures of the natural products, are described. Georg Thieme Verlag Stuttgart.

Biogenetic-type Synthesis of Sesquichamaenol

Paknikar, Shashikumar K.,Naik,Ramanamma

, p. 729 - 733 (2007/10/03)

A hypothetical biosynthetic pathway for the conversion of farnesylpyrophosphate into seaquichamaenol 1, a modified sesquiterpenoid isolated from Chaemaecyparis formosensis Matsum is proposed. The synthesis of 1 which lends experimental support to the prop

Synthesis of phenolic sesquiterpenes via oxidative cleavage of benzocycloalkenols

Ho, Tse-Lok,Yang, Po-Fei

, p. 181 - 192 (2007/10/02)

Phenolic sesquiterpenes including sesquichamaenol, 6-(2-hydroxy-4-methylphenyl)-2-methyl-3-heptanone, and curcuphenol methyl ether have been obtained from oxidative cleavage of bicyclic precursors by treatment with acidic hydrogen peroxide in a process wh

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