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53318-09-5

6-Gingerdiol is a naturally occurring organic compound found in ginger (Zingiber officinale), a popular spice and herbal medicine. It is one of the many bioactive components in ginger, which is known for its anti-inflammatory, antioxidant, and analgesic properties. 6-Gingerdiol is a sesquiterpene, a type of terpene that consists of three isoprene units, and has the molecular formula C15H26O. It is structurally similar to other gingerols and shogaols, which are also present in ginger and contribute to its characteristic aroma and health benefits. Research suggests that 6-gingerdiol may play a role in the various therapeutic effects of ginger, such as reducing inflammation, alleviating nausea, and providing relief from pain.

53318-09-5

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53318-09-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53318-09-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,3,1 and 8 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 53318-09:
(7*5)+(6*3)+(5*3)+(4*1)+(3*8)+(2*0)+(1*9)=105
105 % 10 = 5
So 53318-09-5 is a valid CAS Registry Number.

53318-09-5SDS

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 (3R,5S)-1-(4-hydroxy-3-methoxyphenyl)decane-3,5-diol

1.2 Other means of identification

Product number -
Other names Gingerdiol

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:53318-09-5 SDS

53318-09-5Relevant articles and documents

Synthesis of gingerol and diarylheptanoids

Sabitha, Gowravaram,Srinivas, Chitti,Reddy, Teega Rammohan,Yadagiri, Kurra,Yadav, Jhillu Singh

, p. 2124 - 2133 (2012/03/27)

The synthesis of gingerol 1 and related compounds 2-5 along with diarylheptanoids 6-8 has been accomplished using a Keck allylation, Crimmins' aldol reaction, aldehyde coupling with acetylene, and chelation controlled reductions as the key reactions. The absolute configuration of these molecules was confirmed by preparing their acetonide derivatives and by comparison of the NMR data with natural compounds.

A new method for the demetallation of tricarbonyliron diene complexes by total hydrogenation with Raney nickel. Application to a very short synthesis of (+)-[6]-gingerdiol

Franck-Neumann, Michel,Geoffroy, Philippe,Bissinger, Paul,Adelaide, Sylvie

, p. 6401 - 6404 (2007/10/03)

Demetallation of tricarbonyliron diene complexes is rapidly achieved by treatment with freshly prepared Raney nickel. The ligands which are totally hydrogenated during the decomplexation are easily isolated in high yields, without racemization, if chiral.

GINGERDIOL RELATED COMPOUNDS FROM THE RHIZOMES OF ZINGIBER OFFICINALE

Kikuzaki, Hiroe,Tsai, Saiu-Mei,Nakatani, Nobuji

, p. 1783 - 1786 (2007/10/02)

-Gingerdiol and four analogues, (3R,5S)-5-acetoxy-3-hydroxy-1-(4-hydroxy-3-methoxyphenyl)decane, (3R,5S)-3-acetoxy-5-hydroxy-1-(4-hydroxy-3-methoxyphenyl)decane, (3R,5S)-3,5-diacetoxy-1-(4-hydroxy-3-methoxyphenyl)decane and (3R,5S)-3,5-diacetoxy-1-(3,4

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