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43138-64-3

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43138-64-3 Usage

Uses

Glucofuranose derivative with antiinflammatory, antipyretic, analgesic, and antispasmodic activities.

Check Digit Verification of cas no

The CAS Registry Mumber 43138-64-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,3,1,3 and 8 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 43138-64:
(7*4)+(6*3)+(5*1)+(4*3)+(3*8)+(2*6)+(1*4)=103
103 % 10 = 3
So 43138-64-3 is a valid CAS Registry Number.
InChI:InChI=1/C13H22O6/c1-12(2)15-6-7(17-12)8-9(14-5)10-11(16-8)19-13(3,4)18-10/h7-11H,6H2,1-5H3/t7-,8-,9+,10?,11?/m1/s1

43138-64-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2:5,6-di-O-isopropylidene-3-O-methyl-α-D-glucofuranoside

1.2 Other means of identification

Product number -
Other names 1,2:5,6-Diisopropylidene-3-O-methyl-α-D-glucofuranose

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:43138-64-3 SDS

43138-64-3Relevant articles and documents

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Arnarp et al.

, p. C5 (1975)

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Oligosaccharides Self-Assemble and Show Intrinsic Optical Properties

Yu, Yang,Gim, Soeun,Kim, Dongyoon,Arnon, Zohar A.,Gazit, Ehud,Seeberger, Peter H.,Delbianco, Martina

supporting information, p. 4833 - 4838 (2019/03/26)

Self-assembling peptides and oligonucleotides have given rise to synthetic materials with several applications in nanotechnology. Aggregation of synthetic oligosaccharides into well-defined architectures has not been reported even though natural polysacch

Novel: O -methyl goniofufurone and 7- epi -goniofufurone derivatives: Synthesis, in vitro cytotoxicity and SAR analysis

Francuz, Jovana,Popsavin, Mirjana,Djoki?, Sanja,Koji?, Vesna,Srdi?-Raji?, Tatjana,Rodi?, Marko V.,Jakimov, Dimitar,Popsavin, Velimir

, p. 2017 - 2027 (2019/01/04)

Novel goniofufurone (1) and 7-epi-goniofufurone (2) derivatives bearing a methoxy group at the C-5 and/or C-7 positions were prepared and their in vitro antitumour activity against some human tumour cell lines was evaluated. Some of the analogues displayed powerful antiproliferative effects against the studied tumour cells, but almost all of them were non-cytotoxic toward the normal cells (MRC-5). A SAR study reveals that the introduction of a methoxy group at the C-7 position may increase the antiproliferative effects of the analogues. The most active compounds are 7-O-methyl derivatives of goniofufurone (3) and 7-epi-(+)-goniofufurone (6), which exhibited 1177- and 451-fold higher potencies than the leads 1 and 2 toward the MDA-MB 231 cell line. At the same time, compound 3 is almost 1.5-fold more active than the commercial drug doxorubicin (DOX) against the same cell line. Flow cytometry data confirmed that the cytotoxic effects of these analogues are mediated by apoptosis, additionally revealing that these molecules induced changes in the K562 cell cycle distribution.

Carbohydrate-based N-heterocyclic carbenes for enantioselective catalysis

Henderson, Alexander S.,Bower, John F.,Galan, M. Carmen

supporting information, p. 9180 - 9183 (2015/02/19)

Versatile syntheses of C2-linked and C2-symmetric carbohydrate-based imidazol(in)ium salts from functionalised amino-carbohydrate derivatives are reported. The novel NHCs were ligated to [Rh(COD)Cl]2 and evaluated in Rh-catalysed asymmetric hydrosilylation of ketones with good yields and promising enantioselectivities.

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