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L(+)-tartaric acid, also known as D(-)-tartaric acid, is a naturally occurring organic compound with the chemical formula C4H6O6. It is a white, crystalline solid that is optically active and has a sweet and sour taste. L(+)-tartaric acid is a dicarboxylic acid, meaning it contains two carboxyl groups, and is an important chiral compound, existing in two enantiomeric forms: L(+) and D(-). It is widely used in the food and beverage industry as a flavoring agent, stabilizer, and acidity regulator, as well as in the pharmaceutical and chemical industries for the synthesis of various compounds. The compound can be derived from various sources, including grapes, bananas, and tamarinds, and is also produced through the fermentation of sugars by certain microorganisms.

5866-39-7

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5866-39-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5866-39-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,6 and 6 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5866-39:
(6*5)+(5*8)+(4*6)+(3*6)+(2*3)+(1*9)=127
127 % 10 = 7
So 5866-39-7 is a valid CAS Registry Number.

5866-39-7Relevant academic research and scientific papers

STEREOSELECTIVE SYNTHESIS OF 3,4-DISUBSTITUTED CYCLOPENTANONES AND RELATED COMPOUNDS

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Page/Page column 43, (2010/11/25)

Methods and materials for preparing optically active 3,4-disubstituted cyclopentanones are disclosed. The method includes hydrolyzing one or more compounds represented by Formula (13), or removing an ester moiety from a compound represented by Formula (18).

Double Asymmetric Hydrogenation of Conjugated Dienes Catalysed by Ruthenium-binap Complexes

Muramatsu, Hitoshi,Kawano, Hiroyuki,Ishii, Youichi,Saburi, Masahiko,Uchida, Yasuzo

, p. 769 - 770 (2007/10/02)

Buta-1,3-diene-2,3-dicarboxylic acid is smoothly hydrogenated in the presence of ruthenium-(R)-binap complexes as a catalyst via two consecutive 1,2-hydrogen additions, giving rise to (S,S)-2,3-dimethylsuccinic acid with 98percent diastereoisomeric excess and 96percent enantiomeric excess.

Stereoselective homogeneous hydrogenation. The basis of preferential anti-isomer formation in acyclic systems

Brown, John M.,Cutting, Ian,James, Alun P.

, p. 211 - 217 (2007/10/02)

Directed homogeneous hydrogenation of olefins derived from methyl acrylate proceeds with high selectivity.The reactant must possess a polar substituent at a chiral centre situated in the α'-position; this may be -OH, CO2R or NHCOR.The catalyst should be a cationic chelating rhodium biphosphine complex.In all cases high anti-stereoselectivity is observed in the reduced product, and this can be rationalised by a simple and general model.With an optically active catalyst, efficient kinetic resolution occurs, providing a means of access to optically active acrylates.Experimental details of typical hydrogenation reactions are provided.

HIGHLY DIASTEREOSELECTIVE TANDEM ALKYLATION OF ACYCLIC α,β-UNSATURATED ESTERS BASED ON THE NOVEL USE OF DITHIOACETAL UNIT

Kawasaki, Hisashi,Tomioka, Kiyoshi,Koga, Kenji

, p. 3031 - 3034 (2007/10/02)

Highly diastereoselective tandem alkylation process of acyclic α,β-unsaturated esters was developed based on the novel use of dithioacetal as a stereocontrolling unit.

OXIDATIVE COUPLING REACTIONS UNDER PTC CONDITIONS

Gogte, V.N.,Natu, A.A.,Pandit, V.S.

, p. 4131 - 4134 (2007/10/02)

Succinic acid derivatives have been prepared from cyanohalides under PTC conditions in good yields.

DIMETALATED TERTIARY SUCCINAMIDES. ALKYLATION AND ANNELATION REACTIONS

Mahalanabis, K.K.,Mumtaz, M.,Snieckus, V.

, p. 3971 - 3974 (2007/10/02)

The reactions of dimetalated succinamides 1 with a variety of electrophiles give 2,3-disubstituted adducts (2) with high diasterioselectivity and annelated products (6-9).

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