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1,2:5,6-DI-O-CYCLOHEXYLIDENE-MYO-INOSITOL is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

33021-17-9

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33021-17-9 Usage

Type

Derivative of inositol (a sugar alcohol)

Natural Sources

Found in various plant and animal sources

Usage

Pharmaceutical and medical research

Potential Treatments

a. Polycystic ovary syndrome (PCOS)
b. Gestational diabetes

Investigated Roles

a. Regulating insulin sensitivity
b. Glucose metabolism

Action

Believed to mimic the action of insulin

Functions

a. Promoting glucose uptake
b. Reducing insulin resistance in cells

Therapeutic Benefits

Being studied for managing conditions related to insulin resistance and glucose intolerance

Check Digit Verification of cas no

The CAS Registry Mumber 33021-17-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,0,2 and 1 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 33021-17:
(7*3)+(6*3)+(5*0)+(4*2)+(3*1)+(2*1)+(1*7)=59
59 % 10 = 9
So 33021-17-9 is a valid CAS Registry Number.

33021-17-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (±)-1,2:5,6-di-O-cyclohexylidene-myo-inositol

1.2 Other means of identification

Product number -
Other names (+/-)-2,3:4,5-di-O-cyclohexylidene-myo-inositol

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:33021-17-9 SDS

33021-17-9Relevant academic research and scientific papers

Synthesis of substrate analogues as potential inhibitors for Mycobacterium tuberculosis enzyme MshC

Patel, Krishnakant,Song, Fengling,Andreana, Peter R.

, p. 10 - 18 (2017/11/07)

Mycothiol cysteine ligase (MshC) is a key enzyme in the mycothiol (MSH) biosynthesis and a promising target for developing new anti-mycobacterial compounds. Herein, we report on the synthesis of substrate analogues, as potential inhibitors, for the MshC e

Synthesis of high-performance polyurethanes with rigid 5-6-5-fused ring system in the main chain from naturally occurring myo-inositol

Sudo, Atsushi,Shibata, Yoshiya,Miyamoto, Ayano

, p. 3956 - 3963 (2013/09/02)

A bisketal of myo-inositol was used as a diol-type monomer for synthesis of polyurethanes. The monomer was obtained by treatment of myo-inositol with 1,1-dimethoxycyclohexane in the presence of p-toluenesulfonic acid as a catalyst. The ketalization resulted in the formation of a 5-6-5-fused ring system, which endowed the diol-type monomer with high rigidity. The diol readily reacted with diisocyanate to give the corresponding polyurethane, which exhibited excellent heat resistance due to the rigid 5-6-5 system in the main chain. Copyright

H2SO4-silica: An eco-friendly heterogeneous catalyst for the differential protection of myo-inositol hydroxyl groups

Vibhute, Amol M.,Sureshan, Kana M.

, p. 7321 - 7329 (2013/07/05)

There is enormous interest in myo-inositol derivatives as they serve as precursors for the synthesis of several biologically important phosphoinositols, natural products, catalyst, supramolecular architectures etc. However the presence of six secondary hy

Inositol-phosphate derivatives and method of detecting inositol-1-phosphate

-

Page/Page column 38, (2012/05/20)

The present invention relates to inositol phosphate derivatives, in which the inositol phosphate is substituted with one or two reactive groups G or one or two conjugated substances or molecules M, said reactive group(s) G or said substance(s) or molecule

Synthesis of a glycosylphosphatidylinositol anchor bearing unsaturated lipid chains

Swarts, Benjamin M.,Guo, Zhongwu

scheme or table, p. 6648 - 6650 (2010/07/04)

A GPI anchor bearing unsaturated fatty acid lipid chains (1) was synthesized by a highly convergent strategy employing the para-methoxybenzyl group for permanent hydroxyl protection. The final global deprotection was achieved by an efficient three-step, one-pot procedure to give an 81% isolated yield of the target structure.

First Total Synthesis of Mycothiol and Mycothiol Disulfide

Lee, Sungwon,Rosazza, John P. N.

, p. 365 - 368 (2007/10/03)

(Matrix presented) The first total synthesis of mycothiol and mycothiol disulfide was achieved by linking D-2,3,4,5,6-penta-O-acetyl-myo-inositol, O-(3,4,6-tri-O-acetyl)-2-azido-2-deoxy-α,β-D-glucopyranosyl) trichloroacetimidate, and N,S-diacetyl-L-cysteine and deprotecting peracetylated mycothiol. The first full spectral characterization is reported for underivatized mycothiol. The structure of mycothiol was confirmed by spectral analysis of the known bimane derivative.

First total synthesis of a GPI-anchored peptide

Xue, Jie,Shao, Ning,Guo, Zhongwu

, p. 4020 - 4029 (2007/10/03)

A GPI-anchored dipeptide of sperm CD52 antigen was prepared through a convergent synthesis. First, the dipeptide with its C-terminus free and the GPI with its nonreducing end phosphoeth-anolamine bearing a free amino group were synthesized separately. Then, the two building blocks were coupled with use of EDC/HOBt as the condensation reagent. Finally, the GPI-anchored peptide was deprotected to give the target molecule 1.

Modulation of the inositol 1,4,5-trisphosphate receptor by inositol phosphates

Lu, Pei-Jung,Chen, Ching-Shih

, p. 325 - 328 (2007/10/03)

The mode of recognition at the binding site of the Ins(1,4,5)P3 receptor was assessed by examining the structure-activity relationships of different Ca2+-mobilizing inositol phosphates.

Synthesis of meso-cyclohexa-3,5-diene-1,2-diol derivative from myo-inositol

Mereyala, Hari Babu,Pannala, Madhavi

, p. 2121 - 2124 (2007/10/02)

Synthesis of (meso)1,2-O-cyclohexylidene-cyclohexa-3,4-diene (4) in four steps from myo-inositol and its exclusive conversion to the vinylic epoxide 13 is described.

SYNTHESIS, POTENTIOMETRIC AND 31P-NMR INVESTIGATIONS OF THE IONIZATION STATE AND COMPLEXATION PROPERTIES OF INOSITOL-PHOSPHATES: BIOLOGICAL CONSEQUENCES

Schmitt, Laurent,Bortmann, Patrick,Spiess, Bernard,Schlewer, Gilbert

, p. 147 - 150 (2007/10/02)

The synthesis and the potentiometric studies of inositol-phosphates allow, particularly for Ins(1,4,5)P3, the correlation between the ionization state of the phosphate functions and the binding properties of the inositol-phosphates.

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