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(+)-Diethyl L-tartrate, 98%, Thermo Scientific Chemicals

$90.95 - $511.33

Chemical Identifiers

CAS 87-91-2
Molecular Formula C8H14O6
Molecular Weight (g/mol) 206.19
MDL Number MFCD00009143
InChI Key YSAVZVORKRDODB-UHFFFAOYNA-N
Synonym diethyl l-+-tartrate, 2r,3r-diethyl 2,3-dihydroxysuccinate, l +-diethyl l-tartrate, +-diethyl l-tartrate, diethyl l-tartrate, diethyl-l-tartrate, unii-oq72cpy58z, l-+-tartaric acid diethyl ester, diethyl l-tartarate, tartaric acid, diethyl ester, r,r
PubChem CID 6993580
SMILES CCOC(=O)C(O)C(O)C(=O)OCC
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Products 4
Catalog Number Mfr. No. Quantity Price Quantity  
Catalog Number Mfr. No. Quantity Price Quantity  
AAA1064122
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Thermo Scientific Chemicals
A1064122
100 g N/A
 
AAA1064130
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Thermo Scientific Chemicals
A1064130
250 g N/A
 
AAA1064136
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Thermo Scientific Chemicals
A1064136
500 g N/A
 
AAA106410B
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Thermo Scientific Chemicals
A106410B
1000 g N/A
 
Description

Description

(+)-Diethyl L-tartrate is used as a chiral auxiliary in the Sharpless enantioselective epoxidation of allylic alcohols, for Sharpless-type enantioselective oxidation of sulfides to sulfoxides and as a chiral auxiliary in the enantioselective construction of cyclopropanes from allylic alcohols by an asymmetric Simmons-Smith reaction. It is also used as a chiral reagent in a host of chemical reactions, such as the synthesis of isoquinoline alkaloids and arundic acid, which has been used in acute ischemic stroke therapy.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
(+)-Diethyl L-tartrate is used as a chiral auxiliary in the Sharpless enantioselective epoxidation of allylic alcohols, for Sharpless-type enantioselective oxidation of sulfides to sulfoxides and as a chiral auxiliary in the enantioselective construction of cyclopropanes from allylic alcohols by an asymmetric Simmons-Smith reaction. It is also used as a chiral reagent in a host of chemical reactions, such as the synthesis of isoquinoline alkaloids and arundic acid, which has been used in acute ischemic stroke therapy.

Solubility
Fully miscible in water.

Notes
Keep container tightly sealed. Store in cool, dry conditions in well sealed containers. Incompatible with oxidizing agents.
Specifications

Chemical Identifiers

87-91-2
206.19
YSAVZVORKRDODB-UHFFFAOYNA-N
6993580
C8H14O6
MFCD00009143
diethyl l-+-tartrate, 2r,3r-diethyl 2,3-dihydroxysuccinate, l +-diethyl l-tartrate, +-diethyl l-tartrate, diethyl l-tartrate, diethyl-l-tartrate, unii-oq72cpy58z, l-+-tartaric acid diethyl ester, diethyl l-tartarate, tartaric acid, diethyl ester, r,r
CCOC(=O)C(O)C(O)C(=O)OCC

Specifications

87-91-2
1.205
93°C (199°F)
1.446
100 g
14,3855
Fully miscible in water.
+27° (c=1 in water)
1,4-diethyl 2,3-dihydroxybutanedioate
6993580
98%
17°C
280°C
C8H14O6
MFCD00009143
1727145
diethyl l-+-tartrate, 2r,3r-diethyl 2,3-dihydroxysuccinate, l +-diethyl l-tartrate, +-diethyl l-tartrate, diethyl l-tartrate, diethyl-l-tartrate, unii-oq72cpy58z, l-+-tartaric acid diethyl ester, diethyl l-tartarate, tartaric acid, diethyl ester, r,r
YSAVZVORKRDODB-UHFFFAOYNA-N
CCOC(=O)C(O)C(O)C(=O)OCC
206.19
206.19
(+)-Diethyl L-tartrate
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Safety and Handling

Safety and Handling

GHS H Statement
H227
Combustible liquid.

P210-P264b-P280-P302+P352-P305+P351+P338-P332+P313-P362-P370+P378q-P501c

H227-H315-H319

EINECSNumber : 201-783-3

TSCA : Yes

Recommended Storage : Ambient temperatures

SDS
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RUO – Research Use Only