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62983-70-4

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62983-70-4 Usage

General Description

DI-BETA-D-XYLOPYRANOSYLAMINE, also known as D-Xyloseamine, is a chemical compound belonging to the class of aminosugars. It is a derivative of D-xylose and is commonly used as a building block for the synthesis of various pharmaceuticals and natural products. It has also been studied for its potential anti-inflammatory and immunomodulatory properties. The compound is a white crystalline solid that is soluble in water and has a sweet taste. It is commonly employed in organic chemistry as a chiral auxiliary for the synthesis of complex molecules and as a starting material for the preparation of glycosylated compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 62983-70-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,9,8 and 3 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 62983-70:
(7*6)+(6*2)+(5*9)+(4*8)+(3*3)+(2*7)+(1*0)=154
154 % 10 = 4
So 62983-70-4 is a valid CAS Registry Number.
InChI:InChI=1/C10H19NO8/c12-3-1-18-9(7(16)5(3)14)11-10-8(17)6(15)4(13)2-19-10/h3-17H,1-2H2/t3-,4-,5+,6+,7-,8-,9-,10-/m1/s1

62983-70-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (2R,3R,4S,5R)-2-[[(2R,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]amino]oxane-3,4,5-triol

1.2 Other means of identification

Product number -
Other names -

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:62983-70-4 SDS

62983-70-4Downstream Products

62983-70-4Relevant articles and documents

STRUCTURE AND REARRANGEMENT REACTIONS OF SOME DIGLYCOSYLAMINES

Linek, Kazimir,Alfoeldi, Juraj,Defaye, Jacques

, p. 195 - 206 (1987)

Di-β-D-glucopyranosylamine (2) was prepared by transglycosylation from β-D-glucopyranosylamine.O-Acetylation of 2 led to partial anomerization and the formation of the expected octa-O-acetyl β,β derivative and its α,β anomer in the ratio 1:2,4.Similarly, transglycosylation of β-D-xylopyranosylamine afforded di-β-D-xylopyranosylamine (7).As with 2, the O-acetylation of 7 led to partial anomerization and formation of the hexa-O-acetyl α,β anomer of 7, as well as the expected β,β O-acetylated derivative.O-Deacetylation with ammonia in methanol of (2,3,4-tri-O-acetyl-α-D-xylopyranosyl)(2,3,4-tri-O-acetyl- β-D-xylopyranosyl)amine (7) led to recovery of the β,β-linked starting material.These rearrangement reactions are interpreted in terms of unfavorable nonbonded interactions which modify the thermodynamic equilibrium of the diglycosylamines.

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