What is the (2R,3R,4R,5S,6R)-2-(4-chloro-3-(4-(((S)-tetrahydrofuran-3-yl)oxy)benzyl)phenyl)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol?

(2R,3R,4R,5S,6R)-2-(4-chloro-3-(4-(((S)-tetrahydrofuran-3-yl)oxy)benzyl)phenyl)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol is , while it's Molecular Formula is C 23 H 27 ClO 7 . Empagliflozin α-Anomer is a derivative of Empagliflozin (E521510), a novel, potent and selective SGLT-2 inhibitor, improves glycaemic control syndrome in diabetic rats.

What is the CAS number for (2R,3R,4R,5S,6R)-2-(4-chloro-3-(4-(((S)-tetrahydrofuran-3-yl)oxy)benzyl)phenyl)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol?

The CAS number of (2R,3R,4R,5S,6R)-2-(4-chloro-3-(4-(((S)-tetrahydrofuran-3-yl)oxy)benzyl)phenyl)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol is 1620758-33-9.

What is (2R,3R,4R,5S,6R)-2-(4-chloro-3-(4-(((S)-tetrahydrofuran-3-yl)oxy)benzyl)phenyl)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol (1620758-33-9) used for?

(2R,3R,4R,5S,6R)-2-(4-chloro-3-(4-(((S)-tetrahydrofuran-3-yl)oxy)benzyl)phenyl)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol is a complex organic compound with a unique molecular structure. It is characterized by its stereochemistry, which is defined by the R and S configurations at various carbon atoms. (2R,3R,4R,5S,6R)-2-(4-chloro-3-(4-(((S)-tetrahydrofuran-3-yl)oxy)benzyl)phenyl)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol has potential applications in various fields due to its structural properties and functional groups.

What is the (2R,3R,4R,5S,6R)-2-(4-chloro-3-(4-(((S)-tetrahydrofuran-3-yl)oxy)benzyl)phenyl)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol?

(2R,3R,4R,5S,6R)-2-(4-chloro-3-(4-(((S)-tetrahydrofuran-3-yl)oxy)benzyl)phenyl)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol is , while it's Molecular Formula is C 23 H 27 ClO 7 . Empagliflozin α-Anomer is a derivative of Empagliflozin (E521510), a novel, potent and selective SGLT-2 inhibitor, improves glycaemic control syndrome in diabetic rats.

What is the CAS number for (2R,3R,4R,5S,6R)-2-(4-chloro-3-(4-(((S)-tetrahydrofuran-3-yl)oxy)benzyl)phenyl)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol?

The CAS number of (2R,3R,4R,5S,6R)-2-(4-chloro-3-(4-(((S)-tetrahydrofuran-3-yl)oxy)benzyl)phenyl)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol is 1620758-33-9.

What is (2R,3R,4R,5S,6R)-2-(4-chloro-3-(4-(((S)-tetrahydrofuran-3-yl)oxy)benzyl)phenyl)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol (1620758-33-9) used for?

(2R,3R,4R,5S,6R)-2-(4-chloro-3-(4-(((S)-tetrahydrofuran-3-yl)oxy)benzyl)phenyl)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol is a complex organic compound with a unique molecular structure. It is characterized by its stereochemistry, which is defined by the R and S configurations at various carbon atoms. (2R,3R,4R,5S,6R)-2-(4-chloro-3-(4-(((S)-tetrahydrofuran-3-yl)oxy)benzyl)phenyl)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol has potential applications in various fields due to its structural properties and functional groups.

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1620758-33-9

Product Name：Empagliflozin α-isomer
Molecular Formula：
Purity：99%
Molecular Weight：450.916

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Product Details;

CasNo： 1620758-33-9

Manufacturer supply top purity Empagliflozin α-isomer 1620758-33-9 with GMP standards

Molecular Formula:C₂₃H₂₇ClO₇
Molecular Weight:450.916
Boiling Point:664.5±55.0 °C(Predicted)
PKA:13.23±0.70(Predicted)
Density:1.398±0.06 g/cm3(Predicted)

1620758-33-9 Relevant articles

New Glyflozin Synthesis Method in a Continuous Reaction Process

-

Paragraph 0281; 0282; 0289-0292; 0299-0301, (2021/09/07)

The present invention relates to a metho...

IMPROVED PROCESS FOR THE PREPARATION OF EMPAGLIFLOZIN AND ITS CRYSTALLINE POLYMORPH

-

Page/Page column 4; 9-11, (2021/12/31)

The present invention relates to an impr...

Preparation method of SGLT-2 inhibitor and intermediate

-

, (2021/05/19)

The invention discloses a preparation me...

Synthetic method of empagliflozin

-

Paragraph 0029-0033, (2021/07/24)

The invention belongs to the technical f...

1620758-33-9 Process route

: C₅₁H₄₉ClO₇

: 864070-44-0,1620758-33-9,864070-43-9
empagliflozin

Conditions

Conditions	Yield
With hydrogen; In ethanol; at 75 - 80 ℃; for 20h; under 6000.6 - 6750.68 Torr; Solvent; Inert atmosphere; Autoclave;	93.7%

: 864070-37-1
(2S,3R,4R,5S,6R)-2-(4-chloro-3-(4-hydroxybenzyl)phenyl)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol

: 219823-47-9
(R)-tetrahydrofuran-3-yl 4-methylbenzenesulfonate

: 864070-44-0,1620758-33-9,864070-43-9
empagliflozin

Conditions

Conditions	Yield
With caesium carbonate; In N,N-dimethyl-formamide; at 75 ℃; for 21h;	57%
With caesium carbonate; In N,N-dimethyl-formamide; at 75 ℃; for 18h;	49%
With caesium carbonate; In N,N-dimethyl-formamide; at 75 ℃; for 18h;	49%
With caesium carbonate; at 25 - 40 ℃;
With caesium carbonate; In N,N-dimethyl-formamide; at 30 - 45 ℃; for 24h;	0.55 kg

1620758-33-9 Upstream products

864070-37-1
(2S,3R,4R,5S,6R)-2-(4-chloro-3-(4-hydroxybenzyl)phenyl)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol
112052-11-6
toluene-4-sulfonic acid (S)-(tetrahydrofuran-3-yl)ester
219823-47-9
(R)-tetrahydrofuran-3-yl 4-methylbenzenesulfonate
915095-96-4
methyl-1-C-(4-chloro-3-{4-[(3S)-tetrahydrofuran-3-yloxy]benzyl}phenyl)-D-glucopyranoside

Product Classification

Contact us

1620758-33-9

Product Details;

Manufacturer supply top purity Empagliflozin α-isomer 1620758-33-9 with GMP standards

1620758-33-9 Relevant articles

New Glyflozin Synthesis Method in a Continuous Reaction Process

-

Paragraph 0281; 0282; 0289-0292; 0299-0301, (2021/09/07)

IMPROVED PROCESS FOR THE PREPARATION OF EMPAGLIFLOZIN AND ITS CRYSTALLINE POLYMORPH

-

Page/Page column 4; 9-11, (2021/12/31)

Preparation method of SGLT-2 inhibitor and intermediate

-

, (2021/05/19)

Synthetic method of empagliflozin

-

Paragraph 0029-0033, (2021/07/24)

1620758-33-9 Process route

1620758-33-9 Upstream products

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