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De-O-methylacetovanillochromene is a synthetic organic compound that is primarily used for laboratory research purposes. It is a chemical entity that has garnered interest in scientific studies, although there is currently limited information available in the scientific literature regarding its physical properties or potential applications. As with any laboratory chemical, it is crucial to adhere to safe handling procedures to mitigate potential health risks.

67667-62-3

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67667-62-3 Usage

Uses

Used in Laboratory Research:
De-O-methylacetovanillochromene is used as a research compound for various scientific investigations. Its role in these studies is to provide insights into chemical reactions, mechanisms, or to serve as a starting material for the synthesis of other compounds. De-O-methylacetovanillochromene's specific applications in research are not well-documented, but its presence in the scientific community indicates its potential value in advancing knowledge in chemistry and related fields.

Check Digit Verification of cas no

The CAS Registry Mumber 67667-62-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,6,6 and 7 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 67667-62:
(7*6)+(6*7)+(5*6)+(4*6)+(3*7)+(2*6)+(1*2)=173
173 % 10 = 3
So 67667-62-3 is a valid CAS Registry Number.

67667-62-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(8-Hydroxy-2,2-dimethyl-2H-chromen-6-yl)ethanone

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

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:67667-62-3 SDS

67667-62-3Downstream Products

67667-62-3Relevant academic research and scientific papers

Chemical constituents from the root bark of Rodgersia sambucifolia

Hu, Hao-Bin,Jian, Yu-Feng,Cao, Hong,Zheng, Xu-Dong

, p. 75 - 80 (2007)

A new demethylacetovanillochromene glycoside, 2,2-dimethyl-2H-(8-hydroxy-6- acetyl)-[2,3-b] pyran-8-O-β-D-apiofuranosyl-(1→6)-β-D- glucopyranoside (1), together with twenty-three known compounds, have been isolated from the root bark of Rodgersia sambucifolia. These known compounds include two diterpenoids, three flavonoids, two catechins, four lignans, two benzenoids, two isocoumarins, two steroids and six monoterpene glycosides, which were determined by means of spectral analyses.

6-acetyl-8-hydroxy-2,2-dimethylchromene, an antioxidant in sunflower seeds; Its isolation and synthesis and antioxidant activity of its derivatives

Tsuda, Hideyuki,Ishitani, Youichi,Takemura, Yoshiyuki,Suzuki, Yoshiaki,Kato, Tadahiro

, p. 139 - 142 (2007/10/03)

By the guide of assay toward inhibition of photooxidation of β-carotene, 6-acetyl-8-hydroxy-2,2-dimethylchromene (1) was isolated from sunflower seeds. In addition to 1, the analogous compounds possessing the chromene (chromane) skeleton were synthesized and their antioxidant activities were examined.

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