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2,3-ANHYDRO-4,6-O-BENZYLIDENE-N-(TERT-BUTOXYCARBONYL)-1,5-DEOXY-1,5-IMINO-D-GLUCITOL is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

133697-22-0

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133697-22-0 Usage

Chemical Properties

White Solid

Check Digit Verification of cas no

The CAS Registry Mumber 133697-22-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,6,9 and 7 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 133697-22:
(8*1)+(7*3)+(6*3)+(5*6)+(4*9)+(3*7)+(2*2)+(1*2)=140
140 % 10 = 0
So 133697-22-0 is a valid CAS Registry Number.

133697-22-0SDS

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 2,3-Anhydro-4,6-O-benzylidene-N-(tert-butoxycarbonyl)-1,5-deoxy-1,5-imino-D-glucitol

1.2 Other means of identification

Product number -
Other names [2R-(2|A,4a|A,6a|A,7a|A,7b|A)]-Hexahydro-2-phenyl-5H-1,3-dioxino[5,4-b]oxireno[d]pyridine-5-carboxylic Acid 1,1-Dimethylethyl Ester

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:133697-22-0 SDS

133697-22-0Downstream Products

133697-22-0Relevant academic research and scientific papers

NUCLEOPHILIC OPENING OF N-CARBOALKOXY-2,3-ANHYDRO-1-DEOXYMANNOJIRIMYCIN. A USEFUL METHOD FOR THE SYNTHESES OF 2-, 3- AND 2,3-DISUBSTITUTED 1-DEOXYNOJIRIMYCIN ANALOGS

Khanna, Ish K.,Koszyk, Francis J.,Stealey, Michael A.,Weier, Richard M.,Julien, Janet,et al.

, p. 843 - 878 (2007/10/02)

A useful methodology for the synthesis of a number of 2-, 3- and 2,3-disubstituted deoxynojirimycin analogs is reported.It has been found that the epoxides in stereoselectively synthesized N-carboalkoxy-2,3-anhydro-1-deoxymannojirimycins (4 and 5) react with N-, S- and F-nucleophiles to give a mixture of gluco and altro products.The 3-azido altro compound (12b) yields the desired gluco derivative (40) by oxidation, in situ epimerization at C-3, followed by stereoselective reduction of the carbonyl group.The azido intermediate (12a) affords the 2,3-diazido gluco compound (51) by double inversion at C-3.Attempts have been made to understand the factors contributing to the opening of epoxides (4, 5 and 9) by different nucleophiles.

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