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(4aS,10aR)-3,4,4a,9,10,10a-Hexahydro-7-hydroxy-1,1,4a-trimethyl-8-isopropylphenanthren-2(1H)-one is a complex organic compound with a molecular formula of C20H26O2. It is a hexahydro derivative of phenanthren-2(1H)-one, featuring a hydroxyl group at the 7th position and an isopropyl group at the 8th position. The compound has a unique stereochemistry, with the 4aS and 10aR configurations indicating the spatial arrangement of the atoms. This molecule is characterized by its tricyclic structure, consisting of a phenanthren core with a six-membered and a five-membered ring fused to it. The compound's properties, such as solubility and reactivity, are influenced by its molecular structure and stereochemistry, making it a subject of interest in organic chemistry and potentially in pharmaceutical or materials science applications.

6755-93-7

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6755-93-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6755-93-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,7,5 and 5 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6755-93:
(6*6)+(5*7)+(4*5)+(3*5)+(2*9)+(1*3)=127
127 % 10 = 7
So 6755-93-7 is a valid CAS Registry Number.

6755-93-7SDS

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 totarolone

1.2 Other means of identification

Product number -
Other names 7-oxototarol

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:6755-93-7 SDS

6755-93-7Relevant academic research and scientific papers

Synthesis of antimicrobial natural products targeting FtsZ: (+)-totarol and related totarane diterpenes

Kim, Michelle B.,Shaw, Jared T.

supporting information; experimental part, p. 3324 - 3327 (2010/11/02)

(Equation Presented). An efficient, convergent synthesis of totarol by a diastereoselective epoxide/alkene/arene bicyclization is described. The reported synthesis enables the preparation of related diterpenes totaradiol and totarolone as well as previously unavailable derivatives that exhibit comparable inhibition of the bacterial cell division protein FtsZ.

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