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3-(2,3-dibromo-4,5-dihydroxybenzyl)-3,3a,6-trihydroxytetrahydrofuro[3,2-b]furan-2(3H)-one (non-preferred name) is a complex organic compound belonging to the furofuran derivative class. It features a tetrahydrofuran ring with multiple hydroxyl groups and a benzene ring with bromine substituents. 3-(2,3-dibromo-4,5-dihydroxybenzyl)-3,3a,6-trihydroxytetrahydrofuro[3,2-b]furan-2(3H)-one (non-preferred name) exhibits intriguing biological properties, making it a promising candidate for pharmaceutical applications. However, its complex molecular structure and non-preferred name may lead to its reference by systematic or simplified chemical names in scientific literature and research.

100676-10-6

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100676-10-6 Usage

Uses

Used in Pharmaceutical Industry:
3-(2,3-dibromo-4,5-dihydroxybenzyl)-3,3a,6-trihydroxytetrahydrofuro[3,2-b]furan-2(3H)-one (non-preferred name) is used as a potential pharmaceutical compound for its interesting biological properties. Its unique structural features, including the tetrahydrofuran ring and bromine-substituted benzene ring, contribute to its potential applications in medicinal chemistry.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, 3-(2,3-dibromo-4,5-dihydroxybenzyl)-3,3a,6-trihydroxytetrahydrofuro[3,2-b]furan-2(3H)-one (non-preferred name) serves as a valuable compound for studying its structure-activity relationships and exploring its potential therapeutic effects. The presence of multiple hydroxyl and bromine substituents allows for further chemical modifications and optimization of its pharmacological properties.

Check Digit Verification of cas no

The CAS Registry Mumber 100676-10-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,6,7 and 6 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 100676-10:
(8*1)+(7*0)+(6*0)+(5*6)+(4*7)+(3*6)+(2*1)+(1*0)=86
86 % 10 = 6
So 100676-10-6 is a valid CAS Registry Number.

100676-10-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-[(2,3-dibromo-4,5-dihydroxyphenyl)methyl]-3,6,6a-trihydroxy-3,3a-dihydro-2H-furo[3,2-b]furan-5-one

1.2 Other means of identification

Product number -
Other names Rhodomelol

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:100676-10-6 SDS

100676-10-6Downstream Products

100676-10-6Relevant academic research and scientific papers

Vitamin C in Organic Synthesis: Reaction with p-Hydroxybenzyl Alcohol Derivatives

Poss, Andrew J.,Belter, Randolph K.

, p. 1535 - 1540 (2007/10/02)

The reaction of L-ascorbic acid (1) with p-hydroxybenzyl alcohol (9) yields 2-(p-hydroxybenzyl)-3-ketohexulosonic acid lactone (10).This reaction proceeds by the addition of the conjugate base of ascorbic acid to the protonated quinone methide derived fro

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