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411233-68-6

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411233-68-6 Usage

Molecular Weight

123.152 g/mol

Physical State

Colorless, odorless liquid at room temperature

Solubility

Soluble in water

Applications

a. Organic synthesis
b. Pharmaceutical and agricultural products
c. Chiral building block in the synthesis of pharmaceuticals and agrochemicals
d. Production of flavors, fragrances, and specialty chemicals

Safety Precautions

a. May cause skin and eye irritation
b. Harmful if swallowed or inhaled
c. Handle with care and use appropriate protective equipment

Check Digit Verification of cas no

The CAS Registry Mumber 411233-68-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,1,1,2,3 and 3 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 411233-68:
(8*4)+(7*1)+(6*1)+(5*2)+(4*3)+(3*3)+(2*6)+(1*8)=96
96 % 10 = 6
So 411233-68-6 is a valid CAS Registry Number.

411233-68-6Downstream Products

411233-68-6Relevant articles and documents

QUINOLONE ANTIBACTERIAL AGENTS

-

Page/Page column 104, (2010/02/11)

Compounds of formula (I, II, III, IV, V, and VI) and methods for their preparation are disclosed. Further disclosed are methods of making biologically active compounds of formula (I) as well as pharmaceutically acceptable compositions comprising compounds of formula (I). Compounds of formula (I) as disclosed herein can be used in a variety of applications including use as antibacterial agents.

Microbiological transformations. 47. A step toward a green chemistry preparation of enantiopure (S)-2-, -3-, and -4-pyridyloxirane via an epoxide hydrolase catalyzed kinetic resolution

Genzel,Archelas,Broxterman,Schulze,Furstoss

, p. 538 - 543 (2007/10/03)

The biocatalyzed hydrolytic kinetic resolution of 2-, 3-, and 4-pyridyloxirane by the Aspergillus niger epoxide hydrolase (EH) has been explored. This was used to perform a gram scale preparation of these epoxides of (S) absolute configuration using a process performed at a concentration as high as 10 g/L (82 mM). All three epoxides have been obtained in a nearly enantiopure form (ee > 98%). Interestingly, it was shown that this biotransformation could be achieved using plain water instead of buffer solution, an important improvement as far as downstream processing of an eventual industrial process is concerned. Neither of these substrates could be obtained in reasonable enantiomeric purity and yield using the nowadays most efficient metal-based catalysts.

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