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D-Ribonic acid, .gamma.-lactone, 2,5-bis(4-methylbenzenesulfonate) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

82130-86-7

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82130-86-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82130-86-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,1,3 and 0 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 82130-86:
(7*8)+(6*2)+(5*1)+(4*3)+(3*0)+(2*8)+(1*6)=107
107 % 10 = 7
So 82130-86-7 is a valid CAS Registry Number.

82130-86-7SDS

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 2,5-di-O-tosyl-D-ribono-1,4-lactone

1.2 Other means of identification

Product number -
Other names 2,5-di-O-tosyl-D-ribono lactone

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:82130-86-7 SDS

82130-86-7Relevant academic research and scientific papers

De novo synthesis of 1-deoxythiosugars

Gunasundari, Thanikachalam,Chandrasekaran, Srinivasan

, p. 30 - 35 (2013)

A short and efficient chemical synthesis of biologically potent and novel 1-deoxythiosugars is accomplished. Introduction of sulfur mediated by benzyltriethylammonium tetrathiomolybdate, as a sulfur transfer reagent through nucleophilic double displacemen

A new stereospecific synthesis of 1,2,4-Trideoxy-1,4-imino-D-erythro-pentitol

Malle, Birgitte Molholm,Lundt, Inge,Furneaux, Richard H.

, p. 573 - 583 (2007/10/03)

1,2,4-Trideoxy-1,4-imino-D-erythro-pentitol [(2R,3S)-3-hydroxy-2-hydroxymethylpyrrolidine] (4) was synthesised from 2,5-di-O-tosyl-D-ribono-1,4-lactone in 42 % overall yield. The key steps were deoxygenation at C-2 and a stereospecific inversion of the co

Regioselective tosylation of aldonolactones

Lundt,Madsen

, p. 1129 - 1132 (2007/10/02)

An investigation of the selective di-O-acylation with p-toluenesulfonyl (tosyl) chloride of the four D-pentono-, the eight D-hexono- and D-glycero-D-gulo-heptonolactone has been undertaken, and a number of 2,5-, 2,6- and 2,7-di-O-tosylated lactones have b

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