Lot numbers can be found on the outside label of a product:
Peracetyl Empagliflozin
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CAS No. 915095-99-7
- Cat. No. CS-0010420
- Purity≥98%
- MDL No.MFCD28978546
*For research and further manufacturing use only, not for direct human use.
Structure of 915095-99-7
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General Information
- CAS No. 915095-99-7
- Cat. No. CS-0010420
- Purity ≥98%
- MDL No. MFCD28978546
- Storage 4°C
- Shipping Room temperature in continental US; may vary elsewhere.
- Molecular Formula C₃₁H₃₅ClO₁₁
- Molecular Weight 619.06
- Synonym(s) None
- SMILES ClC1=C(CC2=CC=C(O[C@H]3COCC3)C=C2)C=C([C@H]4[C@H](OC(C)=O)[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@@H](COC(C)=O)O4)C=C1
Description
This tetraacetate derivative features a protected glycosyl scaffold with orthogonal functionalization, enabling selective deprotection and downstream conjugation in complex carbohydrate synthesis. The chlorinated aryl group imparts enhanced lipophilicity and metabolic stability, while the tetrahydrofuran-3-yl ether moiety provides stereochemical control during coupling steps.
Application
(2R,3R,4R,5S,6S)-2-(acetoxymethyl)-6-(4-chloro-3-(4-(((S)-tetrahydrofuran-3-yl)oxy)benzyl)phenyl)tetrahydro-2H-pyran-3,4,5-triyl triacetate serves as a highly functionalized glycosyl donor scaffold, enabling stereoselective glycosylation reactions in complex carbohydrate and glycoconjugate synthesis. The triacetate protection pattern ensures bench stability and facilitates orthogonal deprotection strategies. Its rigid pyran ring framework with multiple chiral centers supports precise stereochemical control in downstream coupling steps.
Safety Information
Download SDS|
GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302
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Precautionary Statements : P264-P270-P330
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Quality Control
Computational Chemistry Data
- TPSA 132.89
- LogP 3.8966
- H_Acceptors 11
- H_Donors 0
- Rotatable_Bonds 10
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Key Words
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