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D-Glucose, 2,3,4,5,6-penta-O-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

14168-89-9

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14168-89-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 14168-89-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,1,6 and 8 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 14168-89:
(7*1)+(6*4)+(5*1)+(4*6)+(3*8)+(2*8)+(1*9)=109
109 % 10 = 9
So 14168-89-9 is a valid CAS Registry Number.

14168-89-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (2R,3S,4R,5R)-2,3,4,5,6-pentamethoxyhexanal

1.2 Other means of identification

Product number -
Other names D-gluco-2,3,4,5,6-Pentamethoxy-hexanal

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:14168-89-9 SDS

14168-89-9Downstream Products

14168-89-9Relevant academic research and scientific papers

Chimeric azalides with functionalized western portions

Waddell, Sherman T.,Eckert, Jeffrey M.,Blizzard, Timothy A.

, p. 2325 - 2332 (2007/10/03)

A series of chimeric azalides which are homologous to the potent azalide antibiotic 9-deoxo-8a-aza-8a-homoerythromycin A (2) in their eastern halves, but which have functionally complex western halves derived from a variety of sources, including carbohydr

REMOVAL OF SUGAR DITHIOACETAL GROUP WITH N-BROMOSUCCINIMIDE

Miljkovic, Momcilo,Dropkin, Daniel,Hagel, Peter,Habash-Marino, Margaret

, p. 11 - 20 (2007/10/02)

Oxidative removal of the dithioacetal group of several protected sugar and 2-acylamido-2-deoxy sugar dialkyl dithioacetals with N-bromosuccinimide in 97percent aqueous acetone or 1:1 (v/v) 2-methyl-2-propanol-acetone was compared with removal with mercury dichloride-mercury(II) oxide or mercury dichloride-cadmium carbonate.In general, removal with N-bromosuccinimide proceeded more rapidly, and, with one exception, yields higher than or equal to those obtained with the method using mercury salt.

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