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100676-10-6

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  • a-L-xylo-3-Hexulofuranosonic acid,2-C-[(2,3-dibromo-4,5-dihydroxyphenyl)methyl]-, g-lactone (9CI)

    Cas No: 100676-10-6

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100676-10-6 Usage

General Description

The chemical "3-(2,3-dibromo-4,5-dihydroxybenzyl)-3,3a,6-trihydroxytetrahydrofuro[3,2-b]furan-2(3H)-one" is a complex organic compound that is commonly known by its non-preferred name. It is a derivative of furofuran, containing a tetrahydrofuran ring with multiple hydroxyl groups and a benzene ring with bromine substituents. This chemical is a potential pharmaceutical compound with interesting biological properties, and its structural features make it suitable for use in medicinal chemistry. However, due to its complex molecular structure and non-preferred name, it may be more commonly referred to by its systematic name or by a simplified chemical name in scientific literature and research applications.

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 articles and documents

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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