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(2S,3S,4R,5R,6S)-6-[[(1S,2R,19R,22S,34S,37R,40R,52S)-5,32-dichloro-52-[3-(dimethylamino)propylcarbamoyl]-2,26,31,44,49-pentahydroxy-22-(methylamino)-21,35,38,54,56,59-hexaoxo-47-[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-7,13,28-trioxa-20,36,39,53,55,58-hexazaundecacyclo[38.14.2.23,6.214,17.219,34.18,12.123,27.129,33.141,45.010,37.046,51]hexahexaconta-3,5,8,10,12(64),14(63),15,17(62),23(61),24,26,29(60),30,32,41(57),42,44,46(51),47,49,65-henicosaen-64-yl]oxy]-3,4-dihydroxy-5-(10-methylundecanoylamino)oxane-2-carboxylic acid(CAS: 171500-79-1)

(2S,3S,4R,5R,6S)-6-[[(1S,2R,19R,22S,34S,37R,40R,52S)-5,32-dichloro-52-[3-(dimethylamino)propylcarbamoyl]-2,26,31,44,49-pentahydroxy-22-(methylamino)-21,35,38,54,56,59-hexaoxo-47-[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-7,13,28-trioxa-20,36,39,53,55,58-hexazaundecacyclo[38.14.2.23,6.214,17.219,34.18,12.123,27.129,33.141,45.010,37.046,51]hexahexaconta-3,5,8,10,12(64),14(63),15,17(62),23(61),24,26,29(60),30,32,41(57),42,44,46(51),47,49,65-henicosaen-64-yl]oxy]-3,4-dihydroxy-5-(10-methylundecanoylamino)oxane-2-carboxylic acid
CAS Number

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Basic Information

Molecular Formula
C88H100Cl2N10O28
Molecular Weight
1816.7 g/mol

Chemical Identifiers

SMILES
CC(C)CCCCCCCCC(=O)NC1C(C(C(OC1OC2=C3C=C4C=C2OC5=C(C=C(C=C5)C(C6C(=O)NC(C7=C(C(=CC(=C7)O)OC8C(C(C(C(O8)CO)O)O)O)C9=C(C=CC(=C9)C(C(=O)N6)NC(=O)C4NC(=O)C1C2=C(C(=CC(=C2)OC2=C(C=CC(=C2)C(C(=O)NC(CC2=CC=C(O3)C=C2)C(=O)N1)NC)O)O)Cl)O)C(=O)NCCCN(C)C)O)Cl)C(=O)O)O)O
InChIKey
KGPGQDLTDHGEGT-FOPUKGCJSA-N

Database References

MDL Number
MFCD09837770

FAQ

This compound is a complex organic molecule with a high molecular weight due to its extensive hydroxyl and amino groups. It crystallizes as a white solid with a melting point of approximately 220°C. Soluble in water and common organic solvents. Chemically, it is reactive towards nucleophiles due to its hydroxyl and amino functionalities, and can undergo esterification and amide formation reactions. Its high polarity and multiple functional groups make it challenging to handle without appropriate chemical protection.
The synthesis of this compound involves multi-step processes including condensation reactions, protection of functional groups, and controlled ring formation. Commonly, it is synthesized using chiral pool synthesis or asymmetric catalysis. The specific method would involve protecting the hydroxyl and amino groups, followed by introduction of the dichloro group and other substituents using appropriate reagents and catalysts. High yields and selectivities are achieved through careful control of reaction conditions and purification steps.
This compound demonstrates potential applications in pharmaceuticals due to its complex structure and functional groups, which can be used in drug discovery and design. It may also be used in the development of new materials in the polymer industry, and in chemical sensors for detecting specific analytes. Its unique properties make it suitable for use in semiconductor research, particularly in organic electronics and optoelectronics.
When handling this compound, safety precautions are essential to prevent exposure and ensure proper laboratory practices. Use personal protective equipment (PPE) such as gloves, lab coat, and safety goggles. Handle in a well-ventilated area or fume hood to minimize inhalation. Avoid skin contact and ingestion. Store in a closed container away from heat and direct sunlight in a secure chemical storage area. Dispose of waste according to local regulations. Always consult the Safety Data Sheet (SDS) for detailed handling instructions and emergency procedures.

Safety Notice

Please verify product specifications and safety data before use. Contact the supplier for detailed safety information.

Always follow proper handling procedures

Contact Information

Contact Person

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