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(S)-2,3-Dihydro-6-(2-hydroxyethyl)-2-hydroxymethyl-5,7-dimethyl-1H-inden-1-one is a complex chemical compound that belongs to the class of ketones. It is characterized by its unique structure, which includes two hydroxyl groups and two methyl groups. As a chiral molecule, it has a non-superimposable mirror image, existing in two enantiomeric forms. (S)-2,3-Dihydro-6-(2-hydroxyethyl)-2-hydroxymethyl-5,7-dimethyl-1H-inden-1-one is a derivative of 1H-inden-1-one and may hold potential applications in various fields, such as pharmaceuticals or as a precursor in chemical synthesis. The presence of hydroxyl groups in its structure suggests that it could exhibit biological activity or reactivity in chemical reactions. Further research is necessary to fully comprehend its properties and potential uses.

35964-50-2

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35964-50-2 Usage

Uses

Used in Pharmaceutical Applications:
(S)-2,3-Dihydro-6-(2-hydroxyethyl)-2-hydroxymethyl-5,7-dimethyl-1H-inden-1-one is used as a potential pharmaceutical compound for [application reason] due to its complex structure and the presence of hydroxyl groups, which may contribute to its biological activity.
Used in Chemical Synthesis:
In the chemical synthesis industry, (S)-2,3-Dihydro-6-(2-hydroxyethyl)-2-hydroxymethyl-5,7-dimethyl-1H-inden-1-one is used as a precursor for [application reason] because of its unique structural features that can be exploited in the synthesis of other complex molecules.
Used in Research and Development:
(S)-2,3-Dihydro-6-(2-hydroxyethyl)-2-hydroxymethyl-5,7-dimethyl-1H-inden-1-one is utilized as a research compound for [application reason] to explore its potential reactivity and biological activity, which could lead to the discovery of new applications in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 35964-50-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,9,6 and 4 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 35964-50:
(7*3)+(6*5)+(5*9)+(4*6)+(3*4)+(2*5)+(1*0)=142
142 % 10 = 2
So 35964-50-2 is a valid CAS Registry Number.
InChI:InChI=1/C14H18O3/c1-8-5-10-6-11(7-16)14(17)13(10)9(2)12(8)3-4-15/h5,11,15-16H,3-4,6-7H2,1-2H3/t11-/m0/s1

35964-50-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name pterosin G

1.2 Other means of identification

Product number -
Other names (2S)-Pterosin G

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:35964-50-2 SDS

35964-50-2Upstream product

35964-50-2Downstream Products

35964-50-2Relevant academic research and scientific papers

Ptesculentoside, a novel norsesquiterpene glucoside from the Australian bracken fern Pteridium esculentum

Fletcher, Mary T.,Hayes, Patrica Y.,Somerville, Michael J.,De Voss, James J.

, p. 1997 - 1999 (2010)

A novel norsesquiterpene glucoside ptesculentoside has been isolated from the Australian bracken Pteridium esculentum, together with the known bracken carcinogen ptaquiloside and lesser amounts of caudatoside. The structure of ptesculentoside is determined by analysis of 1D and 2D NMR spectra, and via its conversion into previously known pterosin G. Crown Copyright

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