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2,5-anhydro-1-deoxy-1-phosphonoaltritol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

86762-89-2

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86762-89-2 Usage

Derived from

Altritol (a sugar alcohol)

Contains

A phosphono group

Usage

As a starting material in the synthesis of various nucleotide analogs

Importance

Valuable building block for the development of new drugs and therapeutic agents

Potential applications

In the field of glycobiology and carbohydrate chemistry, for studying and manipulating biological processes involving carbohydrates and their derivatives.

Check Digit Verification of cas no

The CAS Registry Mumber 86762-89-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,7,6 and 2 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 86762-89:
(7*8)+(6*6)+(5*7)+(4*6)+(3*2)+(2*8)+(1*9)=182
182 % 10 = 2
So 86762-89-2 is a valid CAS Registry Number.
InChI:InChI=1/C6H13O7P/c7-1-3-5(8)6(9)4(13-3)2-14(10,11)12/h3-9H,1-2H2,(H2,10,11,12)/t3-,4-,5-,6+/m1/s1

86762-89-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,5-anhydro-1-deoxy-1-phosphono-D-altritol

1.2 Other means of identification

Product number -
Other names ribose-1-α-methylenephosphonate

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:86762-89-2 SDS

86762-89-2Downstream Products

86762-89-2Relevant academic research and scientific papers

Synthesis of phosphonate and phostone analogues of ribose-1-phosphates

Nasomjai, Pitak,O'Hagan, David,Slawin, Alexandra M. Z.

supporting information; experimental part, (2010/04/22)

The synthesis of phosphonate analogues of ribose-1-phosphate and 5-fluoro-5-deoxyribose-1-phosphate is described. Preparations of both the a- and β-phosphonate anomers are reported for the ribose and 5-fluoro-5- deoxyribose series and a synthesis of the c

2,5-Anhydro-1-deoxy-1-phosphono-D-altritol, an isosteric analogue of α-D-ribofuranose 1-phosphate

Meyer Jr.,Stone,Jesthi

, p. 1095 - 1098 (2007/10/02)

Condensation of tetramethyl methylenebisphosphonate with 2,3-O-isopropylidene-5-O-trityl-D-ribose gave a mixture of 2,5-anhydro-1-deoxy-1-(diethoxyphosphinyl)-2,3-O-isopropylidene-5-O-trityl -D-altritol and -allitol. Separation of the isomers and deprotec

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