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(2R,6S,7S,8R)-7-(1,3-benzodioxol-5-yl)-2,3-dimethoxy-8-methyl-6-(prop-2-en-1-yl)tricyclo[4.2.0.0~2,8~]oct-3-en-5-one is a complex organic molecule with a tricyclic ring structure and multiple functional groups. It features a benzodioxol moiety at the seventh position and a propenyl group at the sixth position of the tricyclic ring. Additionally, it has two methoxy groups at the second and third positions, and a methyl group at the eighth position. (2R,6S,7S,8R)-7-(1,3-benzodioxol-5-yl)-2,3-dimethoxy-8-methyl-6-(prop-2-en-1-yl)tricyclo[4.2.0.0~2,8~]oct-3-en-5-one exhibits stereochemistry with the assigned (2R,6S,7S,8R) configuration, which influences its specific properties, potential uses, and biological activities.

62499-70-1

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62499-70-1 Usage

Uses

Used in Pharmaceutical Industry:
(2R,6S,7S,8R)-7-(1,3-benzodioxol-5-yl)-2,3-dimethoxy-8-methyl-6-(prop-2-en-1-yl)tricyclo[4.2.0.0~2,8~]oct-3-en-5-one can be used as a pharmaceutical compound for its potential biological activities. Its unique structure and functional groups may contribute to its therapeutic effects, making it a candidate for further research and development in the pharmaceutical field.
Used in Chemical Synthesis:
(2R,6S,7S,8R)-7-(1,3-benzodioxol-5-yl)-2,3-dimethoxy-8-methyl-6-(prop-2-en-1-yl)tricyclo[4.2.0.0~2,8~]oct-3-en-5-one can also be used as a starting material or intermediate in the synthesis of other complex organic compounds. Its versatile structure allows for further functionalization and modification, enabling the development of new molecules with specific properties and applications.
Used in Research and Development:
(2R,6S,7S,8R)-7-(1,3-benzodioxol-5-yl)-2,3-dimethoxy-8-methyl-6-(prop-2-en-1-yl)tricyclo[4.2.0.0~2,8~]oct-3-en-5-one serves as a valuable compound for research and development purposes. Its unique structure and stereochemistry make it an interesting subject for studying the relationship between molecular structure and biological activity, as well as for exploring new synthetic routes and methodologies.

Check Digit Verification of cas no

The CAS Registry Mumber 62499-70-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,4,9 and 9 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 62499-70:
(7*6)+(6*2)+(5*4)+(4*9)+(3*9)+(2*7)+(1*0)=151
151 % 10 = 1
So 62499-70-1 is a valid CAS Registry Number.

62499-70-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-allyl-7-(benzo[d][1,3]dioxol-5-yl)-2,3-dimethoxy-8-methyltricyclo[4.2.0.0<sup>2,8</sup>]oct-3-en-5-one

1.2 Other means of identification

Product number -
Other names -

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

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More Details:62499-70-1 SDS

62499-70-1Upstream product

62499-70-1Downstream Products

62499-70-1Relevant academic research and scientific papers

Piperhancins A and B, Two Pairs of Antineuroinflammatory Cycloneolignane Enantiomers from Piper hancei

Yang, Fan,Su, Bao-Jun,Hu, Ya-Jie,Liu, Jin-Long,Li, Hua,Wang, Ya-Qi,Liao, Hai-Bing,Liang, Dong

, p. 5284 - 5291 (2021)

Two pairs of cycloneolignane enantiomers, piperhancins A and B (1 and 2, respectively), along with two enantiomeric pairs of biosynthetic related neolignanes, hancinone C (3) and piperhancin C (4), were isolated from the stems of Piper hancei. Compound 1 is an unprecedented 1′,2:1,2′-dicyclo-8,3′-neolignane. Their structures and absolute configurations were elucidated by spectroscopic analyses, X-ray diffraction, and electronic circular dichroism calculations. Among all of the isolates, compounds (+)-1, (-)-1, (+)-2, (-)-2, and (+)-3 could significantly inhibit the production of nitric oxide secreted by lipopolysaccharide (LPS)-induced neuroinflammation in BV-2 microglial cells, with IC50 values of 1.1-26.3 μM. In addition, compound (-)-1 could decrease the mRNA levels of iNOS, IL-6, and TNF-α induced by LPS in BV-2 microglial cells.

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