Di-p-anisoyl-D-tartaric acid CAS#: 191605-10-4; ChemWhat Code: 1026567

IdentificationPhysical DataSpectra
Route of Synthesis (ROS)Safety and HazardsOther Data

Identification

Product NameDi-p-anisoyl-D-tartaric acid
IUPAC Name(2S,3S)-2,3-bis[(4-methoxybenzoyl)oxy]butanedioic acid
Molecular StructureDi-p-anisoyl-D-tartaric-acid-CAS-191605-10-4
CAS Registry Number 191605-10-4
MDL NumberMFCD07368366
Synonyms191605-10-4
(2S,3S)-2,3-Bis((4-methoxybenzoyl)oxy)succinic acid
(+)-Di-p-anisoyl-D-tartaric Acid
Butanedioic acid, 2,3-bis[(4-methoxybenzoyl)oxy]-, (2S,3S)-
(+)-Di-4-Anisoyl-D-tartaric acid
Dibenzoyl-(+)-P-methoxy-D-tartaric acid
(2S,3S)-2,3-BIS(4-METHOXYBENZOYLOXY)BUTANEDIOIC ACID
MFCD07368366
(+)-Bis(4-methoxybenzoyl)-D-tartaric Acid
EC 606-247-6
SCHEMBL935315
(2S,3S)-2,3-bis[(4-methoxybenzoyl)oxy]butanedioic acid
KWWCVCFQHGKOMI-HOTGVXAUSA-N
DTXSID701304214
AKOS016843093
AC-3424
CS-W008144
AS-11927
A4227
D3490
Di-(p-Methoxybenzoyl)-D-(+)-Tartaric Acid
H10779
EN300-7377917
(2S,3S)-2,3-bis(4-methoxybenzoyloxy)succinic acid
(2S,3S)-2,3-Bis((4-methoxybenzoyl)oxy)succinicacid
Molecular FormulaC20H18O10
Molecular Weight418.3
InChIInChI=1S/C20H18O10/c1-27-13-7-3-11(4-8-13)19(25)29-15(17(21)22)16(18(23)24)30-20(26)12-5-9-14(28-2)10-6-12/h3-10,15-16H,1-2H3,(H,21,22)(H,23,24)/t15-,16-/m0/s1
InChI KeyKWWCVCFQHGKOMI-HOTGVXAUSA-N 
Isomeric SMILESCOC1=CC=C(C=C1)C(=O)O[C@@H]([C@@H](C(=O)O)OC(=O)C2=CC=C(C=C2)OC)C(=O)O

Physical Data

AppearanceWhite Powder

Spectra

No data available


Route of Synthesis (ROS)

No data available


Safety and Hazards

Pictogram(s)exclamation-mark
SignalWarning
GHS Hazard StatementsH315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]
H319 (100%): Causes serious eye irritation [Warning Serious eye damage/eye irritation]
Precautionary Statement CodesP264, P264+P265, P280, P302+P352, P305+P351+P338, P321, P332+P317, P337+P317, and P362+P364
(The corresponding statement to each P-code can be found at the GHS Classification page.)

Source: European Chemicals Agency (ECHA)
License Note: Use of the information, documents and data from the ECHA website is subject to the terms and conditions of this Legal Notice, and subject to other binding limitations provided for under applicable law, the information, documents and data made available on the ECHA website may be reproduced, distributed and/or used, totally or in part, for non-commercial purposes provided that ECHA is acknowledged as the source: “Source: European Chemicals Agency, http://echa.europa.eu/”. Such acknowledgement must be included in each copy of the material. ECHA permits and encourages organisations and individuals to create links to the ECHA website under the following cumulative conditions: Links can only be made to webpages that provide a link to the Legal Notice page.
License URL: https://echa.europa.eu/web/guest/legal-notice
Record Name: (1-Cyano-2-ethoxy-2-oxoethylidenaminooxy)dimethylamino-morpholino-carbenium hexafluorophosphate
URL: https://echa.europa.eu/information-on-chemicals/cl-inventory-database/-/discli/details/213446
Description: The information provided here is aggregated from the “Notified classification and labelling” from ECHA’s C&L Inventory. Read more: https://echa.europa.eu/information-on-chemicals/cl-inventory-database


Other Data

TransportationUnder the room temperature, in container tightly sealed; Protect from light.
HS Code
StorageUnder the room temperature, in container tightly sealed; Protect from light.
Shelf Life2 years
Market Price
Use Pattern
D-(+)-Di-p-methoxybenzoyl-tartaric acid (DPMTA) is a chiral compound, is commonly used in organic chemistry and pharmaceutical chemistry as a chiral resolving agent to separate racemic mixtures. It can form diastereomeric salts with racemic compounds, which can then be separated by crystallization or chromatography techniques. As a chiral catalyst or chiral ligand, DPMTA is used in asymmetric synthesis reactions to enhance enantioselectivity. This is particularly important in the synthesis of chiral drugs or chiral materials.

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Caming Pharmaceutical Limitedhttp://www.caming.com/
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