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Di-p-anisoyl-D-tartaric acid CAS 191605-10-4
- Identification

- Properties

- Safety Data

- Specifications & Other Information

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Identification

CAS Number

191605-10-4

Name

Di-p-anisoyl-D-tartaric acid CAS 191605-10-4

Synonyms

(2S,3S)-2,3-bis(4-methoxybenzoyloxy)butanedioic acid(2S,3S)-2,3-Bisbernsteinsäure (2S,3S)-2,3-Bisbutanedioic acid(2S,3S)-2,3-Bissuccinic acid (2S,3S)-2,3-Bis{oxy}butanedioic acid(S,S)-Di-p-anisoyltartaric acid191605-10-4 1OR DVOYVQYVQOVR DO1 &&(2S,3S)- Form 3227682 Acide (2S,3S)-2,3-bissuccinique Butanedioic acid, 2,3-bis-, (2S,3S)- Di-p-anisoyl-D-tartaric acid (2S,3S)-2,3-bis(4-methoxyphenylcarbonyloxy)butanedioic acid(2S,3S)-2,3-bisbutanedioic acid 98%Jsp003934MFCD07368366 O,O'-Di-p-anisoyl-D-tartaric acidOR-4444PubChem6043SCHEMBL935315

SMILES

COC1=CC=C(C=C1)C(=O)O((C(=O)O)OC(=O)C2=CC=C(C=C2)OC)C(=O)O

StdInChI

InChI=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

StdInChIKey

KWWCVCFQHGKOMI-HOTGVXAUSA-N

Molecular Formula

C20H18O10

Molecular Weight

418.351

MDL Number

MFCD07368366

Properties

Appearance

White Powder

Safety Data

Symbol

GHS07

Signal Word

Warning

Hazard statements

H302, H315, H319, H332, H335

Precautionary Statements

P261, P280, P305, P338, P351

WGK Germany

3

MSDS Download

Specifications and Other Information of Our Di-p-anisoyl-D-tartaric acid CAS 191605-10-4

Purity

98% min

Specific Rotation

+165° ~ +171°

Water

≤0.5%

Shelf Lif

2 years

Storage

Store at room temperature, in container tightly sealed; Protect from light.

Known Application

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.

Links

This product is developed by our R&D company Caming Pharmaceutical Limited (http://www.caming.com/).

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Fill out our inquiry form and one of our experts will be in touch with you shortly.
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