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(5S)-5-(3-O-benzyl-1,2-O-isopropylidene-α-D-xylo-tetrafuranos-4-yl)-3-ethoxycarbonyl-2-isoxazoline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

118374-38-2

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118374-38-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 118374-38-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,8,3,7 and 4 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 118374-38:
(8*1)+(7*1)+(6*8)+(5*3)+(4*7)+(3*4)+(2*3)+(1*8)=132
132 % 10 = 2
So 118374-38-2 is a valid CAS Registry Number.

118374-38-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (5S)-5-(3-O-benzyl-1,2-O-isopropylidene-α-D-xylo-tetrafuranos-4-yl)-3-ethoxycarbonyl-2-isoxazoline

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:118374-38-2 SDS

118374-38-2Downstream Products

118374-38-2Relevant academic research and scientific papers

Synthesis of Higher Monosaccharides using Nitrile Oxide-Isoxazoline Chemistry

Paton, R. Michael,Young, Anne A.

, p. 132 - 134 (2007/10/02)

Octose, nonose and decose derivatives 1, 2, 11, 12 and 18-21 have been synthesised by a sequence involving cycloaddition of sugar nitrile oxides to sugar alkenes, and reductive hydrolytic cleavage of the resulting 2-isoxazolines.

Cycloaddition of nitrile oxides to 3-O-benzyl-5,6-dideoxy-1,2-O-isopropylidene-α-D-ribo-hex-5-enofuranose

Blake, Alexander J.,Gould, Robert O.,McGhie, Karen E.,Paton, R. Michael,Reed, David,et al.

, p. 461 - 474 (2007/10/02)

Benzonitrile oxide and ethoxycarbonylformonitrile oxide cyclo-added to the title compound to afford a mixture of 3-substituted (phenyl or ethoxycarbonyl)(5R)- (6) and (5S)-5-(3-O-benzyl-1,2-O-isopropylidene-α-D-ribo-tetrofuranos-4-yl)-2-isoxazoline (7).Th

Face Selectivity of the Nitrile Oxide Cycloaddition to Unsaturated Sugars

Amici, De Marco

, p. 793 - 798 (2007/10/02)

Nitrile oxides cycloadd to unsaturated sugars 1a-h, to give the anti adduct with 73.5-96.8percent ?-facial stereoselectivity.The highest values of face selectivity were observed with dipolarophiles bearing an ether group in the homoallylic position.This f

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