51432-61-2 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule of the compound.
Explanation
1,2,3-Propanetriol, 1-benzoate, (R)is formed by the esterification reaction between 1,2,3-propanetriol (a triol) and benzoic acid.
Explanation
The (R)designation indicates that the compound has a specific chiral configuration, meaning it is a non-superimposable mirror image of its enantiomer.
Explanation
1,2,3-Propanetriol, 1-benzoate, (R)is used as a preservative and flavor enhancer in these industries due to its ability to inhibit the growth of microorganisms and improve taste and aroma.
Explanation
The compound is also utilized in the production of cosmetics and personal care products, likely due to its preservative properties and ability to enhance the sensory experience of these products.
Explanation
1,2,3-Propanetriol, 1-benzoate, (R)has antimicrobial properties, which help prevent the growth of bacteria, fungi, and other microorganisms in various products.
Explanation
The compound is used to enhance the taste and aroma of food products, making them more appealing to consumers.
Explanation
The ester linkage is formed through the reaction between the hydroxyl groups of 1,2,3-propanetriol and the carboxyl group of benzoic acid, creating a covalent bond.
Ester formation
Reaction of 1,2,3-propanetriol and benzoic acid
Chiral configuration
(R)-
Applications
Pharmaceutical and food industries
Additional uses
Cosmetics and personal care products
Inhibition of microorganisms
Growth inhibition
Flavor enhancement
Taste and aroma improvement
Chemical structure
Ester linkage between 1,2,3-propanetriol and benzoic acid
Check Digit Verification of cas no
The CAS Registry Mumber 51432-61-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,4,3 and 2 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 51432-61:
(7*5)+(6*1)+(5*4)+(4*3)+(3*2)+(2*6)+(1*1)=92
92 % 10 = 2
So 51432-61-2 is a valid CAS Registry Number.
51432-61-2Relevant articles and documents
A novel method for preparation of optically active α-monobenzoyl glycerol via lipase-catalyzed asymmetric transesterification of glycerol
Kato, Yasuo,Fujiwara, Isao,Asano, Yasuhisa
, p. 3207 - 3210 (1999)
One-step synthesis of optically active α-monobenzoyl glycerol is described by lipase-catalyzed transesterification of benzoate derivatives with glycerol in 1,4-dioxane.
Synthesis of enantiomerically pure (R)-and (S)-1-benzoyloxypropane-2,3-diol and revision of the stereochemical outcome of the Candida antarctica lipase-catalyzed benzoylation of glycerol
Casati, Silvana,Ciuffreda, Pierangela,Santaniello, Enzo
, p. 658 - 661 (2011/07/08)
Enantiomerically pure (R)- and (S)-1-benzoyloxypropane-2,3-diol have been prepared from (S)-(+)-2,2-dimethyl-1,3-dioxolane-4-methanol and used as reference compounds to correct the reported stereochemical outcome of the Candida antarctica lipase (CAL)-cat
Microbial asymmetric reduction of α-hydroxyketones in the anti-Prelog selectivity
Tsujigami, Toshikuni,Sugai, Takeshi,Ohta, Hiromichi
, p. 2543 - 2549 (2007/10/03)
Yamadazyma farinosa IFO 10896 was found to reduce α-hydroxyketones bearing a phenyl ring to give optically active diols with anti-Prelog selectivity. The distance between the carbonyl group and the phenyl ring was shown to have an interesting effect on the reactivity and selectivity of the enzyme system.
