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263155-11-9

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  • D-Glycero-D-galacto-Non-2-enonicacid, 4-(acetylamino)-2,6-anhydro-3,4-dideoxy-

    Cas No: 263155-11-9

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  • 4-ACETYLAMINO-2,6-ANHYDRO-3,4-DIDEOXY-D-GLYCERO-D-GALACTONON-2-ENONIC ACID

    Cas No: 263155-11-9

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263155-11-9 Usage

Chemical Properties

White Solid

Uses

A potential inhibitor of virus sialidase.

Check Digit Verification of cas no

The CAS Registry Mumber 263155-11-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,3,1,5 and 5 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 263155-11:
(8*2)+(7*6)+(6*3)+(5*1)+(4*5)+(3*5)+(2*1)+(1*1)=119
119 % 10 = 9
So 263155-11-9 is a valid CAS Registry Number.
InChI:InChI=1/C11H17NO8/c1-4(14)12-5-2-7(11(18)19)20-10(8(5)16)9(17)6(15)3-13/h2,5-6,8-10,13,15-17H,3H2,1H3,(H,12,14)(H,18,19)/t5?,6-,8?,9-,10?/m1/s1

263155-11-9SDS

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 (2S,3R,4R)-4-acetamido-3-hydroxy-2-[(1R,2R)-1,2,3-trihydroxypropyl]-3,4-dihydro-2H-pyran-6-carboxylic acid

1.2 Other means of identification

Product number -
Other names (2S,3R,4R)-4-ACETAMIDO-3-HYDROXY-2-((1R,2R)-1,2,3-TRIHYDROXYPROPYL)-3,4-DIHYDRO-2H-PYRAN-6-CARBOXYLIC ACID

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:263155-11-9 SDS

263155-11-9Downstream Products

263155-11-9Relevant articles and documents

Novel practical synthesis of Kdn2en and its C-4 nitrogen-modified derivatives

Sun, Xue-Long,Sato, Noriko,Kai, Toshitsugu,Furuhata, Kimio

, p. 1 - 6 (2007/10/03)

A practical synthesis of Kdn2en and 4-amino-4-deoxy-Kdn2en has been achieved via a key intermediate, methyl 4,5,7,8,9-penta-O-acetyl-2,6-anhydro- 3-deoxy-D-glycero-D-galacto-non-2-enonate, which has been prepared from Kdn in three steps in 91% overall yield. (C) 2000 Elsevier Science Ltd.

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