16088-60-1 Usage
Description
[S,(+)]-1-Bromo-2-propanol is a chiral compound characterized by its molecular formula of C3H7BrO. It presents as a white to light brown solid at room temperature and is recognized for its applications in organic synthesis, particularly in the production of pharmaceuticals, dyes, and other organic compounds. This chemical also exhibits antimicrobial properties, which extend its utility in the development of disinfectants and antiseptics.
Uses
Used in Pharmaceutical Industry:
[S,(+)]-1-Bromo-2-propanol is used as a key reagent in the synthesis of various pharmaceutical compounds. Its chiral nature allows for the creation of specific drug molecules with desired therapeutic effects, contributing to the development of novel medications.
Used in Dye Industry:
In the dye industry, [S,(+)]-1-Bromo-2-propanol is utilized as an intermediate in the production of different types of dyes. Its unique chemical structure enables the creation of a wide range of colorants used in various applications, such as textiles, plastics, and printing inks.
Used in Disinfectant and Antiseptic Formulation:
Due to its antimicrobial properties, [S,(+)]-1-Bromo-2-propanol is used as an active ingredient in the formulation of disinfectants and antiseptics. It helps in the development of products that effectively kill or inhibit the growth of microorganisms, promoting better hygiene and reducing the spread of infections.
Used in Organic Synthesis:
[S,(+)]-1-Bromo-2-propanol is employed as a versatile reagent in organic synthesis, allowing for the creation of a diverse array of organic compounds. Its use in this field is crucial for the development of new materials and chemicals with various applications across different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 16088-60-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,0,8 and 8 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 16088-60:
(7*1)+(6*6)+(5*0)+(4*8)+(3*8)+(2*6)+(1*0)=111
111 % 10 = 1
So 16088-60-1 is a valid CAS Registry Number.
16088-60-1Relevant articles and documents
Synthesis of optically active 2s-, and 7s-methyl-1.6-dioxa-spiro[4.5] decane, the pheromone components of Paravespula vulgaris (L.), from S-ethyl lactate.
Hintzer,Weber,Schurig
, p. 55 - 58 (1981)
(-)-2S, 5RS-1 and (-]-7S, 5S-2 are obtained from S-ethyl lactate 4 and their absolute configuration is thus directly correlated. Accurate enantiomeric compositions of intermediates and products were measured by complexation gas chromatography on nickel-, and manganese-bis-3-heptafluorobutyryl-1R-camphorate, 3. It could be conclusively established that the syntheses proceed with a high degree of preservation of configuration.
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Spassky,N.,Sigwalt,P.
, p. 3541 - 3544 (1968)
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Optical resolution, absolute configuration, and activity of the enantiomers of proxyphylline
Selvig,Ruud Christensen,Aasen
, p. 1514 - 1518 (1983)
The enantiomers of proxyphylline have been separated via their corresponding camphanates. Synthesis of (+)-proxyphylline from theophylline and (S)-propylene oxide derived from (S)-lactic acid established the absolute configuration of the (+) and (-) isomer as S and R, respectively. The activity of the enantiomers as cyclic nucleotide phosphodiesterase inhibitors was tested in human lung tissue homogenate. No differences were found either between the two enantiomers or between the enantiomers and racemic proxyphylline.
Enantiotopic group differentiation and kinetic resolution: Asymmetric reduction of meso-1,3-dihalides
Michael Chong,Sokoll, Kenneth K.
, p. 879 - 882 (2007/10/02)
Asymmetric reduction of 1,3-dihalides derived from glycerol occurs with moderate levels of enantiotopic group differentiation. A concomitant kinetic resolution increases the enantiometric purity of the initial product.
Asymmetric Reduction of Trifluoromethyl and Methyl Ketones by Yeast; An Improved Method
Bucciarelli, Maria,Forni. Arrigo,Moretti, Irene,Torre, Giovanni
, p. 897 - 899 (2007/10/02)
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