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76410-46-3

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76410-46-3 Usage

Chemical compound

6-deoxy-6-fluorohex-2-ulofuranosyl 6-deoxy-6-fluorohexopyranoside

Molecular structure

Contains hexose sugars and fluorine atoms

Properties

Unique combination of sugar and fluorine moieties, potential applications in medicinal chemistry and biochemistry

Potential uses

Glycoside, starting material for synthesis of complex molecules

Need for further research

To fully understand properties and potential applications of the compound

Check Digit Verification of cas no

The CAS Registry Mumber 76410-46-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,4,1 and 0 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 76410-46:
(7*7)+(6*6)+(5*4)+(4*1)+(3*0)+(2*4)+(1*6)=123
123 % 10 = 3
So 76410-46-3 is a valid CAS Registry Number.

76410-46-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(fluoromethyl)-6-[5-(fluoromethyl)-3,4-dihydroxy-2-(hydroxymethyl)oxolan-2-yl]oxyoxane-3,4,5-triol

1.2 Other means of identification

Product number -
Other names 6,6'-dideoxy-6,6'-difluorosucrose

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:76410-46-3 SDS

76410-46-3Downstream Products

76410-46-3Relevant articles and documents

SYNTHESIS OF 6,6'-DIDEOXY-6,6'-DIFLUOROSUCROSE

Zikopoulos, John N.,Eklund, Steven H.,Robyt, John F.

, p. 245 - 252 (2007/10/02)

The chemical synthesis of 6,6'-dideoxy-6,6'-difluorosucrose was accomplished in five steps: (a) tritylation of C-6,1' and -6' of sucrose; (b) benzoylation of 6,1',6'-tri-O-tritylsucrose; (c) detritylation with mild acid; (d) fluorination at C-6 and -6' with diethylaminosulfur trifluoride (DAST); and (e) debenzoylation.The resulting compound was chromatographically pure.The structure was established by (13)C and (19)F-n.m.r. spectrometry and by elemental analysis.

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