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16784-00-2

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  • (2S)-7-amino-2,5-dihydroxy-2,4-dimethylbenzo[e][1]benzofuran-1,6,9-trione

    Cas No: 16784-00-2

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16784-00-2 Usage

General Description

The chemical "(2S)-7-amino-2,5-dihydroxy-2,4-dimethyl-benzo[e]benzofuran-1,6,9-trione" is a complex organic compound with a molecular formula C16H13NO6. It is a derivative of benzo[e]benzofuran-1,6,9-trione, which is a naturally occurring compound with potential biological activities. The presence of amino and hydroxyl groups in the chemical structure suggests possible interactions with proteins and enzymes in biological systems. (2S)-7-amino-2,5-dihydroxy-2,4-dimethyl-benzo[e]benzofuran-1,6,9-trione may have potential pharmaceutical applications, including as an anti-cancer, anti-inflammatory, or anti-microbial agent. However, further studies are needed to fully understand its properties and potential uses.

Check Digit Verification of cas no

The CAS Registry Mumber 16784-00-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,7,8 and 4 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 16784-00:
(7*1)+(6*6)+(5*7)+(4*8)+(3*4)+(2*0)+(1*0)=122
122 % 10 = 2
So 16784-00-2 is a valid CAS Registry Number.

16784-00-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S)-7-amino-2,5-dihydroxy-2,4-dimethylbenzo[e][1]benzofuran-1,6,9-trione

1.2 Other means of identification

Product number -
Other names Chromophoric moiety of rifamycins

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:16784-00-2 SDS

16784-00-2Downstream Products

16784-00-2Relevant articles and documents

Synthetic studies of rifamycins. VII. A facile synthesis of the aromatic chromophore of rifamycin S through a rifamycin W aromatic segment

Nakata,Wada,Tatsuta,Kinoshita

, p. 1801 - 1806 (2007/10/02)

The intact aromatic chromophore of rifamycin S, 7-amino-2,5-dihydroxy-2,4-dimethyl-naphtho[2,l-b]furan-1,6,9-(2H)-trion e, was synthesized through the rifamycin W aromatic segment, 1-[5,8-dimethoxy-2,4-bis-(methoxymethoxy)-3-methyl-6-nitro-l-naphthyl]- l-propanone which was prepared in 9 steps and 29.6% overall yield from 2,6-bis(benzyloxy)-3,5-dibromotoluene and furan.

Concerning rifamycin S. Reactions of the ansa ring

Kump,Bickel

, p. 2323 - 2347 (2007/10/09)

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