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10256-24-3

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  • o-Nitrophenyl β-D-Xylopyranoside 2',3',4'-Triacetate

    Cas No: 10256-24-3

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10256-24-3 Usage

Chemical Properties

Off-White Solid

Uses

2’-Nitrophenyl 2,3,4-Tri-O-acetyl-β-D-xylopyranoside (cas# 10256-24-3) is a compound useful in organic synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 10256-24-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,2,5 and 6 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 10256-24:
(7*1)+(6*0)+(5*2)+(4*5)+(3*6)+(2*2)+(1*4)=63
63 % 10 = 3
So 10256-24-3 is a valid CAS Registry Number.

10256-24-3SDS

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-Nitrophenyl 2,3,4-tri-O-acetyl-b-D-xylopyranoside

1.2 Other means of identification

Product number -
Other names 2`-Nitrophenyl 2,3,4-Tri-O-acetyl-Beta-D-xylopyranoside

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

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Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:10256-24-3 SDS

10256-24-3Relevant articles and documents

Synthesis of 2- and 4-nitrophenyl β-glycosides of β-(1 → 4)-D-xylo-oligosaccharides of dp 2-4

Takeo,Ohguchi,Hasegawa,Kitamura

, p. 231 - 244 (2007/10/03)

2- and 4-Nitrophenyl β-D-xylopyranosides (4 and 5) were transformed, via dibutyltin oxide-mediated acylation, into the corresponding 2,3-di-O-benzoyl derivatives 11 and 15. Xylobiose and xylotriose were easily isolated by charcoal column chromatography from a commercially available material and converted into the di- and trisaccharide methyl 1-thio-β-glycosides 36 and 37. The 2- and 4-nitrophenyl β-glycosides of the β-(1 → 4)-D-xylo-oligosaccharides of dp 2-4 were synthesized by N-iodosuccinimide-silver triflate-promoted condensation using 11 and 15 as the glycosyl acceptors and ethyl 1-thio-β-D-xylopyranoside triacetate 16, 36, and 37 as the glycosyl donors. Also described are an improved preparation of 4 and 5, and the synthesis of 1-naphthyl β-D-xylopyranoside, as well as an alternative approach to the 2- and 4-nitrophenyl β-xylobiosides.

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