16741-03-0 Usage
Chemical structure
A complex chemical compound with multiple acetyl and sulfonyl groups attached to a six-carbon sugar derivative.
Function
Used as a protecting agent for hydroxyl groups in carbohydrates, preventing unwanted reactions with other chemical compounds.
Protection mechanism
Acetyl groups protect hydroxyl groups, while sulfonyl groups provide additional protection and stabilization.
Applications
Commonly used in organic synthesis as a reagent or intermediate in the production of various pharmaceuticals, agrochemicals, and other specialty chemicals.
Utility in research
Useful in the study of carbohydrate chemistry and as a tool for the manipulation of sugar molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 16741-03-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,7,4 and 1 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 16741-03:
(7*1)+(6*6)+(5*7)+(4*4)+(3*1)+(2*0)+(1*3)=100
100 % 10 = 0
So 16741-03-0 is a valid CAS Registry Number.
16741-03-0Relevant articles and documents
ON THE SULFONYLATION OF DIETHYL GALACTARATE: SOME STRUCTURAL CORRECTIONS - SYNTHESIS AND CHARACTERISATION OF DERIVATIVES OF DIETHYL 2,5-DIHYDROXYHEXA-2,4-DIENOATE
Saarloos, Tanny J. van,Regeling, Henk,Zwanenburg, Binne,Chittenden, Gordon J. F.
, p. 1007 - 1016 (2007/10/02)
The structure of one of the major products resulting from the treatment of diethyl galactarate (2) with an excess of p-toluenesulfonyl chloride in pyridine has been shown to be diethyl 2,5-ditosyloxyhexa-2,4-dienoate (5) rather than hex-3-enoate 1 propose
