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(2R,3R,4S,5R,6S)-3,4,5-trihydroxy-2-(hydroxymethyl)-6-[C-[(2S)-2-hydroxypent-4-enyl]-N-sulfonatooxy-carbonimidoyl]sulfanyl-oxane is a complex organic molecule characterized by its unique stereochemistry and diverse functional groups. It features a ring structure composed of six carbon atoms, to which are attached multiple hydroxyl and a hydroxymethyl group, along with a sulfonatooxy-carbonimidoyl moiety. The presence of these functional groups suggests potential for biological activity, and the specific arrangement of atoms indicates that (2R,3R,4S,5R,6S)-3,4,5-trihydroxy-2-(hydroxymethyl)-6-[C-[(2S)-2-hydro xypent-4-enyl]-N-sulfonatooxy-carbonimidoyl]sulfanyl-oxane may possess distinct stereochemical properties. This intricate chemical composition could make it a candidate for various applications in fields such as medicine and industry.

19764-03-5

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19764-03-5 Usage

Uses

Used in Pharmaceutical Industry:
(2R,3R,4S,5R,6S)-3,4,5-trihydroxy-2-(hydroxymethyl)-6-[C-[(2S)-2-hydroxypent-4-enyl]-N-sulfonatooxy-carbonimidoyl]sulfanyl-oxane is used as a potential pharmaceutical agent for its possible biological activity due to the presence of multiple hydroxyl and sulfonatooxy-carbonimidoyl groups. These functional groups may allow the compound to interact with biological targets, making it a candidate for the development of new drugs.
Used in Chemical Research:
In the field of chemical research, (2R,3R,4S,5R,6S)-3,4,5-trihydroxy-2-(hydroxymethyl)-6-[C-[(2S)-2-hydroxypent-4-enyl]-N-sulfonatooxy-carbonimidoyl]sulfanyl-oxane serves as a subject of study for understanding the effects of stereochemistry on molecular properties and reactivity. Its complex structure provides opportunities to explore various aspects of organic chemistry, including synthesis, conformational analysis, and potential reactions with other molecules.
Used in Material Science:
(2R,3R,4S,5R,6S)-3,4,5-trihydroxy-2-(hydroxymethyl)-6-[C-[(2S)-2-hydroxypent-4-enyl]-N-sulfonatooxy-carbonimidoyl]sulfanyl-oxane may also find applications in material science, where its unique structure and functional groups could be leveraged to create new materials with specific properties. For instance, its hydroxyl groups could be involved in the formation of hydrogen bonds, potentially contributing to the development of novel polymers or other advanced materials.

Check Digit Verification of cas no

The CAS Registry Mumber 19764-03-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,7,6 and 4 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 19764-03:
(7*1)+(6*9)+(5*7)+(4*6)+(3*4)+(2*0)+(1*3)=135
135 % 10 = 5
So 19764-03-5 is a valid CAS Registry Number.
InChI:InChI=1/C12H21NO10S2/c1-2-3-6(15)4-8(13-23-25(19,20)21)24-12-11(18)10(17)9(16)7(5-14)22-12/h2,6-7,9-12,14-18H,1,3-5H2,(H,19,20,21)/p-1/t6-,7+,9+,10-,11+,12-/m0/s1

19764-03-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name gluconapoleiferin(1?)

1.2 Other means of identification

Product number -
Other names -

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

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More Details:19764-03-5 SDS

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