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2-Heptene-1,5,6-triol,2-[(1S,3R,4R)-4-ethenyl-4-methyl-3-(1-methylethenyl)cyclohexyl]-6-methyl-,(2Z,5R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

139579-30-9

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139579-30-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 139579-30-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,9,5,7 and 9 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 139579-30:
(8*1)+(7*3)+(6*9)+(5*5)+(4*7)+(3*9)+(2*3)+(1*0)=169
169 % 10 = 9
So 139579-30-9 is a valid CAS Registry Number.

139579-30-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name lobatrientriol

1.2 Other means of identification

Product number -
Other names (Z)-(R)-2-((1S,3R,4R)-3-Isopropenyl-4-methyl-4-vinyl-cyclohexyl)-6-methyl-hept-2-ene-1,5,6-triol

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:139579-30-9 SDS

139579-30-9Relevant academic research and scientific papers

Synthetic study of marine lobane diterpenes. Enantioselective syntheses of lobatrienolide and lobatrientriol from (+)-nopinone

Kato, Michiharu,Kosugi, Hiroshi,Ichiyanagi, Tsuyoshi,Yamabe, Osamu

, p. 783 - 788 (2007/10/03)

Michiharu Kato,. The first enantioselective syntheses of highly oxygenated lobane diterpenes, (+)-lobatrienolide 4 and (+)-lobatrientriol 5, have been achieved, starting with (4R,5R)-1-acetoxy-4-isopropenyl-5-methyl-5-vinyl-cyclohex-1-ene 10b which itself has been prepared from (+)-nopinone 7 as a versatile building block toward the asymmetric synthesis of natural products.

Structures and Absolute Configurations of New Lobane Diterpenoids from the Okinawan Soft Coral Sinularia flexibilis

Hamada, Toshiyuki,Kusumi, Takenori,Ishitsuka, Midori O.,Kakisawa, Hiroshi

, p. 33 - 36 (2007/10/02)

Three new diterpenoids possessing lobane skeleton have been isolated from the Okinawan soft coral of Sinularia flexibilis.Their structures and absolute configurations have been established by chemical transformations as well as spectroscopic analysis.

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