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7506-68-5

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7506-68-5 Usage

General Description

2,3,4,6-Tetramethyl-D-glucose is a synthetic chemical compound that is widely used in various scientific research and industrial applications. It belongs to the family of glucose derivatives and is specifically modified with four methyl groups at the 2nd, 3rd, 4th, and 6th carbon positions of the glucose molecule. This modification enhances the compound's stability and solubility, making it useful in applications such as biochemical assays, metabolic studies, and as a reference standard in analytical chemistry. 2,3,4,6-Tetramethyl-D-glucose also serves as a valuable tool for studying carbohydrate metabolism and transport in biological systems. Its unique structure and properties make it an important tool in the fields of biochemistry and chemical biology.

Check Digit Verification of cas no

The CAS Registry Mumber 7506-68-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,0 and 6 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7506-68:
(6*7)+(5*5)+(4*0)+(3*6)+(2*6)+(1*8)=105
105 % 10 = 5
So 7506-68-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H20O6/c1-12-5-6-7(13-2)8(14-3)9(15-4)10(11)16-6/h6-11H,5H2,1-4H3

7506-68-5SDS

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 2,3,4,6-TETRAMETHYL-D-GLUCOSE

1.2 Other means of identification

Product number -
Other names 2,3,4',6-TETRACB UNLABELED

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:7506-68-5 SDS

7506-68-5Downstream Products

7506-68-5Relevant articles and documents

Antibacterial activity of a triterpenoid saponin from the stems of Caesalpinia pulcherrima Linn.

Asati, Nidhi,Yadava

, p. 499 - 507 (2017/09/30)

A new compound 1 was isolated from the methanolic extract of the stems of the Caesalpinia pulcherrima Linn. along with a reported compound (2) 3-O-β-D-glucopyranosyl-(1→4)-β-D-xylopyranosyl-(1→3)-α-L-rhamnopyranosyl-(1→2)-α-L-arabinopyranosyl hederagenin 28-O-β-D-glucopyranosyl-(1→6)-β-D-glucopyranosyl ester. The new compound 1 has m.p. 272–274°C, m.f. C46H74O17, [M]+ m/z 898. It was characterised as 3-O-β-D-glucopyranosyl-(1→4)-α-L-arabinopyranosyl hederagenin 28-O-β-D- xylopyranosyl ester by various colour reactions, chemical degradations and spectral analyses. Antibacterial activity of compound 1 was screened against various Gram-positive and Gram-negative bacteria and showed significant results.

Microwave-accelerated methylation of starch

Singh, Vandana,Tiwari, Ashutosh

, p. 151 - 154 (2008/09/18)

A novel microwave-accelerated method for methylating soluble starch is described. Soluble starch could be fully methylated in 72% yield within 4.66 min using iodomethane and 30% potassium hydroxide under microwave irradiation. The completely methylated starch thus obtained was hydrolyzed with 60% HCO2H for 1.5 min under 80% MW power, followed by 0.05 M H2SO4 for 2.0 min under 100% MW power. The partially methylated monosaccharides were separated by preparative paper chromatography and identified by their melting points and optical rotations.

New Phenolic Components from Dalbergia Volubilis

Chawla, H. Mohindra,Johny, C. J.,Mittal, Ram S.

, p. 82 - 87 (2007/10/02)

Phytochemical examination of non green branches of Dalbergia volubilis on extensive column and preparative thin layer chromatography yielded twelve compounds eight of which are already known compounds and were identified as sitosterol, 7-hydroxy-4-methyl-coumarin, dalbergin, biochanin-A, umbelliferone, p-hydroxy cinnamic acid, kaempferol and quercetin-3-O-glucoside.The other four compounds were new natural products, three of which were identified as novel 4-phenyl-2H-1-benzopyran-2-ones while the fourth one was a new 12a-hydroxy rotenoid.The structure of these new compounds has been established on the basis of chemical and spectral evidences and through derivatization, as 4',7-dihydroxy-3'-methoxy-4-phenyl-2H-1-benzopyran-2-one, 3',7-dihydroxy-4',5-dimethoxy-2H-1-benzopyran-2-one, 3',7-dihydroxy4',5-dimethoxy-6-formyl-2H-1-benzopyran-2-one and a complex rotenoid determined to be as (VII).The co-occurence of 4-methyl-2H-1-benzopyran-2-ones, 4-phenyl-2H-1-benzopyran-2-ones, isoflavones and rotenoids is of interest from biogenetic considerations.

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