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(3R)-4,4aβ,5,6,7,8-Hexahydro-3-hydroxy-4β-methyl-6α-isopropenylnaphthalen-2(3H)-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

55051-94-0

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55051-94-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55051-94-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,0,5 and 1 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 55051-94:
(7*5)+(6*5)+(5*0)+(4*5)+(3*1)+(2*9)+(1*4)=110
110 % 10 = 0
So 55051-94-0 is a valid CAS Registry Number.
InChI:InChI=1/C14H20O2/c1-8(2)10-4-5-11-7-13(15)14(16)9(3)12(11)6-10/h7,9-10,12,14,16H,1,4-6H2,2-3H3/t9-,10+,12-,14+/m0/s1

55051-94-0SDS

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 (+)-glutinosone

1.2 Other means of identification

Product number -
Other names Glutinoson

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:55051-94-0 SDS

55051-94-0Downstream Products

55051-94-0Relevant academic research and scientific papers

The Structure and Configuration of (+)-Glutinosone and (+)-Oxyglutinosone

Murai, Akio,Taketsuru, Hirofumi,Yagihashi, Fujio,Katsui, Nobukatsu,Masamune, Tadashi

, p. 1045 - 1048 (2007/10/02)

The structure elucidation of (+)-glutinosone and (+)-oxyglutinosone, antifungal norsesquiterpenes qualified as phytoalexins in diseased tobacco leaves and in diseased potato tubers, respectively, is described.

The Synthesis of (+/-)-Glutinosone

Murai, Akio,Taketsuru, Hirofumi,Masamune, Tadashi

, p. 1049 - 1056 (2007/10/02)

The synthesis of (+/-)-glutinosone, an antifungal norsesquiterpene from Nicotiana Glutinosa infected with tobacco mosaic virus, is described.It has been completed by two processes, one being based on the Robinson annelation method and another on a modification of the Dastur procedure.

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