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Home/Compounds/Pharmaceutical Intermediate/Di-p-toluoyl-D-tartaric acid monohydrate
C20H20O9
404.4 g/mol
Pharmaceutical Intermediate

(2R,3R)-2,3-Bis((4-methylbenzoyl)oxy)succinic acid hydrate

CAS71607-32-4EC615-312-8
Category
Pharmaceutical Intermediate
Compound Class
Ester
Primary Use
Pharmaceutical Intermediate

(2R,3R)-2,3-bis[(4-methylbenzoyl)oxy]butanedioic acid hydrate is a chiral compound used in the pharmaceutical industry as an intermediate for producing chiral resolving agents. Its structure contains two carboxylic acid groups, two ester groups, and aromatic rings, and it exists as a hydrate.

Chiral resolving agent intermediatePharmaceutical intermediate for enantiomer separation

Content scope: Information here supports chemical identification and industrial supply, research, and manufacturing contexts. It is not a therapeutic claim, medical advice, or drug-use instructions.

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Related Compounds

StrongSame Parent

(-)-Di-p-toluoyl-L-tartaric acid

CAS32634-66-5

pharmaceutical intermediate

StrongSame Parent

(2R,3R)-2,3-Bis[(4-methylbenzoyl)oxy]butanedioic acid compd. with (3R,4R)-N,4-dimethyl-1-(phenylmethyl)-3-piperidinamine

CAS477600-71-8

pharmaceutical intermediate

ReferenceSame Category

2-Methoxy-4-amino-5-ethylthiobenzoic acid

CAS71675-86-0

pharmaceutical intermediate

ReferenceSame Category

4-amino-2-methoxy-5-(methylthio)benzoic acid

CAS71675-98-4

pharmaceutical intermediate

ReferenceSame Category

4-Amino-5-(methanesulfonyl)-2-methoxybenzoic acid

CAS71675-99-5

pharmaceutical intermediate

ReferenceSame Category

4-Amino-N-[(1-ethylpyrrolidin-2-yl)methyl]-5-(methanesulfonyl)-2-methoxybenzene-1-carboximidic acid

CAS71676-00-1

pharmaceutical intermediate

Referencestereoisomer of

(+)-ditoluoyltartaric acid

CAS32634-68-7

research compound

Referencestereoisomer of

Di-p-toluoyl-D-tartaric acid monohydrate

CAS71607-31-3

pharmaceutical intermediate

Identifiers
IUPAC Name

(2R,3R)-2,3-bis[(4-methylbenzoyl)oxy]butanedioic acid;hydrate

InChIKey

FOTRUJUPLHRVNU-QNBGGDODSA-N

SMILES

CC1=CC=C(C=C1)C(=O)O[C@H]([C@H](C(=O)O)OC(=O)C2=CC=C(C=C2)C)C(=O)O.O

Synonyms (4)

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