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4-O-acetyl-1,5-anhydro-2,3,6-tri-O-ethylglucitol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

119554-98-2

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119554-98-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 119554-98-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,9,5,5 and 4 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 119554-98:
(8*1)+(7*1)+(6*9)+(5*5)+(4*5)+(3*4)+(2*9)+(1*8)=152
152 % 10 = 2
So 119554-98-2 is a valid CAS Registry Number.
InChI:InChI=1/C14H26O6/c1-5-16-8-11-14(20-10(4)15)13(18-7-3)12(9-19-11)17-6-2/h11-14H,5-9H2,1-4H3

119554-98-2SDS

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 [4,5-diethoxy-2-(ethoxymethyl)oxan-3-yl] acetate

1.2 Other means of identification

Product number -
Other names 4-O-Acetyl-1,5-anhydro-2,3,6-tri-O-ethylglucitol

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:119554-98-2 SDS

119554-98-2Downstream Products

119554-98-2Relevant academic research and scientific papers

Analysis of the positions of substitution of acetate and butyrate groups in cellulose acetate-butyrate by the reductive-cleavage method

Yu, Nanxiong,Gray, Gary R.

, p. 225 - 231 (1998)

The degree of substitution (ds) and the distribution pattern of the two ester substituents in commercial samples of cellulose acetate-butyrate (CAB) were determined by sequential neutral methylation, direct reductive cleavage and in situ acetylation. When

SYNTHESIS AND MASS SPECTRA OF 4-O-ACETYL-1,5-ANHYDRO-2,3,6-TRI-O-ETHYL-D-GLUCITOL AND THE POSITIONAL ISOMER OF 4-O-ACETYL-1,5-ANHYDRO-DI-O-ETHYL-O-METHYL-D-GLUCITOL AND 4-O-ACETYL-1,5-ANHYDRO-O-ETHYL-DI-O-METHYL-D-GLUCITOL

Zeller, Samuel G.,D'Ambra, Anello J.,Rice, Michael J.,Gray, Gary R.

, p. 53 - 62 (2007/10/02)

Reductive cleavage of fully methylated, partially O-ethylated cellulose or fully ethylated, partially O-methylated cellulose and subsequent acetylation had previously been shown to produce 4-O-acetyl-1,5-anhydro-2,3,6-tri-O-methyl-, -6-Oethyl-2,3-di-O-methyl-, -3-O-ethyl-2,6-di-O-methyl-, -2-O-ethyl-3,6-di-O-methyl-, -2,3,di-O-ethyl-6-O-methyl-, -2,6-di-O-ethyl-3-O-methyl-, -3,6-di-O-ethyl-2-O-methyl-, and -2,3,6-tri-O-ethyl-D-glucitol.Described herein is the independent synthesis of these derivatives, except for the first (which had been reported); and their (1)H-n.m.r. spectra, chemical-ionization (NH3) mass spectra, and electron-impact mass spectra are tabulated.

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