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(-)-(2R,3R)-cis-5,7-bis(benzyloxy)-2-[3,4,5-tris(benzyloxy)phenyl]chroman-3-yl 3,4,5-tris(benzyloxy)benzoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

332386-77-3

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332386-77-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 332386-77-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,2,3,8 and 6 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 332386-77:
(8*3)+(7*3)+(6*2)+(5*3)+(4*8)+(3*6)+(2*7)+(1*7)=143
143 % 10 = 3
So 332386-77-3 is a valid CAS Registry Number.

332386-77-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (-)-(2R,3R)-cis-5,7-bis(benzyloxy)-2-[3,4,5-tris(benzyloxy)phenyl]chroman-3-yl 3,4,5-tris(benzyloxy)benzoate

1.2 Other means of identification

Product number -
Other names 5,7,3',4',5'-penta-O-benzyl-3-O-(3,4,5-tri-O-benzylgalloyl)epigallocatechin

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:332386-77-3 SDS

332386-77-3Relevant academic research and scientific papers

Design and synthesis of epigallocatechin (EGC) analogs selective to inhibit α-amylase over α-glucosidases via the incorporation of caffeine acid and its derivatives

Chen, Wenming,Zhou, Cui,Chen, Jiansheng,Wang, Meizhu,Zhou, Fang,Wang, Chunmei,Zhang, Xu,Zhou, Wen

, (2021/12/13)

Natural products are a promising and underappreciated reservoir for the preferred chemical scaffolds in the search of antidiabetic drugs. In this study twenty-one EGC-based derivatives selective to inhibit human pancreatic α-amylase (HPA), the enzyme at t

Epigallocatechin gallate derivatives preparation method

-

Paragraph 0035; 0037; 0044; 0045, (2018/11/22)

The invention mainly aims at achieving lipid-solubility transformation of epigallocatechin gallate which is polyhydroxy, good in water solubility and low in bioavailability, including three ways, namely encapsulating hydroxyl with different anhydrides so

NOVEL COMPOSITIONS AND METHODS FOR THE TREATMENT OF LEIOMYOMA

-

Paragraph 0087, (2017/12/27)

This invention provides novel compositions and methods for the treatment of leiomyoma. In some other aspects, this invention provides novel compositions and methods comprising prodrugs of (-)-epigallocatechin-3-gallate (EGCG) and prodrugs of (-)-EGCG anal

The design, synthesis and biological evaluation of pro-EGCG derivatives as novel anti-vitiligo agents

Wang, Siyu,Jin, Rong,Wang, Ruiquan,Hu, Yongzhou,Dong, Xiaowu,Xu, Ai e

, p. 106308 - 106315 (2016/11/23)

With the aim of overcoming the instability and poor membrane permeability of epigallocatechin-3-gallate (EGCG), a series of prodrugs of EGCG and its derivatives (pro-EGCGs) were designed and synthesized, and their protective effect on melanocytes against

Structure-activity relationship of oligomeric flavan-3-ols: Importance of the upper-unit B-ring hydroxyl groups in the dimeric structure for strong activities

Hamada, Yoshitomo,Takano, Syota,Ayano, Yoshihiro,Tokunaga, Masahiro,Koashi, Takahiro,Okamoto, Syuhei,Doi, Syoma,Ishida, Masahiko,Kawasaki, Takashi,Hamada, Masahiro,Nakajima, Noriyuki,Saito, Akiko

, p. 18870 - 18885 (2015/11/27)

Proanthocyanidins, which are composed of oligomeric flavan-3-ol units, are contained in various foodstuffs (e.g., fruits, vegetables, and drinks) and are strongly biologically active compounds. We investigated which element of the proanthocyanidin structu

The synthesis of methylated epigallocatechin gallate

Lai, Ronghui,Zhao, Wenfang,Huang, Yahui,Zhou, Wen,Wu, Chunlan,Lai, Xingfei,Zhao, Wenxia,Zhang, Ming

, p. 472 - 475 (2015/12/26)

Synthesis of methylated epigallocatechin gallate from (-)-epigallocatechin gallate and propylgallate was accomplished using a benzyl (Bn) group as a protecting group for phenols. This methodology provided (-)-epigallocatechin-3-(4-O-methylgallate), which

Semisynthesis of fluoro-substituted benzoates of Epi-gallocatechin

Qin, Xu Long,Li, Xue Min,Yuan, Jian,Chen, Di,Jiang, Tao,Dou, Q. Ping,Chan, Tak Hang,Wan, Sheng Biao

experimental part, p. 3524 - 3531 (2012/09/25)

In the present study, four fluoro-substituted benzoates of epi-gallocatechin (EGC) were prepared through a semisynthetic strategy, and the yield of benzylation of epi-gallocatechin gallate (-)-EGCG was improved by using freshly purified (-)-EGCG as starting material and a mild base of K 2CO3. All structures of new compounds were characterized by 1H NMR, 13C NMR, high-resolution mass spectrometry, and optical rotation.

General synthesis of epi-series catechins and their 3-gallates: Reverse polarity strategy

Ohmori, Ken,Yano, Takahisa,Suzuki, Keisuke

supporting information; experimental part, p. 2693 - 2696 (2010/08/21)

A general synthetic route to the epi-series catechins was developed based on the reverse polarity strategy. Aromatic nucleophilic substitution reaction followed by the sulfinyl-metal exchange and cyclization enabled stereo-controlled access to various members of epi-series catechins and their 3-gallates.

Synthesis of (2R,3R)-epigallocatechin-3-O-(4-hydroxybenzoate), a novel catechin from Cistus salvifolius, and evaluation of its proteasome inhibitory activities

Osanai, Kumi,Huo, Congde,Landis-Piwowar, Kristin R.,Dou, Q. Ping,Chan, Tak Hang

, p. 7565 - 7570 (2008/09/18)

The total and semi syntheses of (2R,3R)-epigallocatechin-3-O-(4-hydroxybenzoate), a novel catechin from Cistus salvifolius, were accomplished. The proteasome inhibition and cytotoxic activities of the synthetic compound and its acetyl derivative were stud

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