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Benzoic acid,3,4,5-trihydroxy-,(1R,2S)-2-[(2R,3R)-3,4-dihydro-5,7-dihydroxy-3-[(3,4,5-trihydroxybenzoyl)oxy]-2-(3,4,5-trihydroxyphenyl)-2H-1-benzopyran-8-yl]-2-(3,4,5-trihydroxyphenyl)-1-[(2,4,6-trihydroxyphenyl)methyl]ethylester (9CI) is a complex organic compound characterized by its intricate chemical structure. It features multiple benzene rings and hydroxyl groups, along with chiral centers, which give it unique properties and potential applications in various fields. Benzoic acid,3,4,5-trihydroxy-,(1R,2S)-2-[(2R,3R)-3,4-dihydro-5,7-dihydroxy-3-[(3,4,5-trihydroxybenzoyl)oxy]-2-(3,4,5-trihydroxyphenyl)-2H-1-benzopyran-8-yl]-2-(3,4,5-trihydroxyphenyl)-1-[(2,4,6-trihydroxyphenyl)methyl]ethylester (9CI)'s chemical properties and uses are likely to be the focus of ongoing research and exploration due to its distinctive molecular architecture.

121795-66-2

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121795-66-2 Usage

Uses

Used in Pharmaceutical Industry:
Benzoic acid,3,4,5-trihydroxy-,(1R,2S)-2-[(2R,3R)-3,4-dihydro-5,7-dihydroxy-3-[(3,4,5-trihydroxybenzoyl)oxy]-2-(3,4,5-trihydroxyphenyl)-2H-1-benzopyran-8-yl]-2-(3,4,5-trihydroxyphenyl)-1-[(2,4,6-trihydroxyphenyl)methyl]ethylester (9CI) is used as a pharmaceutical compound for its potential therapeutic effects. Benzoic acid,3,4,5-trihydroxy-,(1R,2S)-2-[(2R,3R)-3,4-dihydro-5,7-dihydroxy-3-[(3,4,5-trihydroxybenzoyl)oxy]-2-(3,4,5-trihydroxyphenyl)-2H-1-benzopyran-8-yl]-2-(3,4,5-trihydroxyphenyl)-1-[(2,4,6-trihydroxyphenyl)methyl]ethylester (9CI)'s unique structure and functional groups may contribute to its bioactivity, making it a candidate for the development of new drugs or drug delivery systems.
Used in Chemical Research:
In the field of chemical research, Benzoic acid,3,4,5-trihydroxy-,(1R,2S)-2-[(2R,3R)-3,4-dihydro-5,7-dihydroxy-3-[(3,4,5-trihydroxybenzoyl)oxy]-2-(3,4,5-trihydroxyphenyl)-2H-1-benzopyran-8-yl]-2-(3,4,5-trihydroxyphenyl)-1-[(2,4,6-trihydroxyphenyl)methyl]ethylester (9CI) serves as a subject of study for understanding its chemical properties, reactivity, and potential applications. Its complex structure and chirality may offer insights into new synthetic pathways, catalysis, or the development of novel materials.
Used in Material Science:
Benzoic acid,3,4,5-trihydroxy-,(1R,2S)-2-[(2R,3R)-3,4-dihydro-5,7-dihydroxy-3-[(3,4,5-trihydroxybenzoyl)oxy]-2-(3,4,5-trihydroxyphenyl)-2H-1-benzopyran-8-yl]-2-(3,4,5-trihydroxyphenyl)-1-[(2,4,6-trihydroxyphenyl)methyl]ethylester (9CI) may be utilized in material science for the development of new materials with specific properties. Its hydroxyl groups and aromatic rings could be exploited to create polymers, coatings, or other materials with tailored characteristics.

Check Digit Verification of cas no

The CAS Registry Mumber 121795-66-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,1,7,9 and 5 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 121795-66:
(8*1)+(7*2)+(6*1)+(5*7)+(4*9)+(3*5)+(2*6)+(1*6)=132
132 % 10 = 2
So 121795-66-2 is a valid CAS Registry Number.

121795-66-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name assamicain A

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 -
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More Details:121795-66-2 SDS

121795-66-2Relevant academic research and scientific papers

Tannins and Related Compounds. LXXVII. Novel Chalcan-flavan Dimers, Assamicains A, B and C, and a New Flavan-3-ol and Proanthocyanidins from the Fresh Leaves of Camellia sinensis L. var. assamica KITAMURA

Hashimoto, Fumio,Nonaka, Gen-ichiro,Nishioka, Itsuo

, p. 77 - 85 (2007/10/02)

Three novel chalcan-flavan dimers, assamicains A (1), B (2) and C (3), and a new flavan-3-ol (14) and proanthocyanidins (19,20) have been isolated, together with the known flavan-3-ols (4-13), proanthocyanidins (15-18,21), theasinensins (22-24) and hydrolyzable tannins (25,26), from the fresh leaves of Camellia sinensis var. assamica (Camelliaceae), and their structures have been established on the basis of spectroscopic evidence in conjunction with thiolytic degradation and enzymatic hydrolysis. - Keywords: Camellia sinensis var. assamica; Camelliaceae; polyphenol; assamicain; chalcan-flavan dimer; proanthocyanidin; theasinensin; flavan-3-ol; hydrolyzable tannin; black tea

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