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

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-Bis[(4-methoxybenzoyl)oxy]bernsteinsäure [Ger­man] [ACD/IUPAC Name]
(2S,3S)-2,3-Bis[(4-methoxybenzoyl)oxy]butanedioic acid
(2S,3S)-2,3-Bis[(4-methoxybenzoyl)oxy]succinic acid [ACD/IUPAC Name]
(2S,3S)-2,3-Bis{[(4-methoxyphenyl)carbonyl]oxy}butanedioic acid
(S,S)-Di-p-anisoyltartaric acid
191605-10-4 [RN]
1OR DVOYVQYVQOVR DO1 &&(2S,3S)- Form [WLN]
3227682 [Beil­stein]
Acide (2S,3S)-2,3-bis[(4-méthoxybenzoyl)oxy]succinique [French] [ACD/IUPAC Name]
Butane­dioic acid, 2,3-bis[(4-methoxybenzoyl)oxy]-, (2S,3S)- [ACD/​Index Name]
Di-p-anisoyl-D-tar­­tar­ic acid [ACD/IUPAC Name]
(2S,3S)-2,3-bis(4-methoxyphenylcarbonyloxy)butanedioic acid
(2S,3S)-2,3-bis[(4-methoxyphenyl)carbonyloxy]butanedioic acid
[191605-10-4] [RN]
98%
Jsp003934
MFCD07368366 [MDL num­ber]
O,O’-Di-p-anisoyl-D-tartaric acid
OR-4444
PubChem6043
SCHEMBL935315

SMILES

COC1=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

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

exclamation-mark-jpgGHS07

Sig­nal Word

Warn­ing

Haz­ard statements

H302, H315, H319, H332H335

Pre­cau­tion­ary Statements

P261, P280, P305, P338P351

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.

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

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