124600-38-0 Usage
Explanation
Different sources of media describe the Explanation of 124600-38-0 differently. You can refer to the following data:
1. A carboxylic acid derivative is a compound that has undergone a modification or substitution of the carboxylic acid group (-COOH).
3. Dioxolane ring
2. A dioxolane ring is a four-membered ring containing two oxygen atoms, which is part of the structure of this compound.
4. Three methyl groups
5. 4S-cis configuration
3. The 4S-cis configuration indicates the stereochemistry of the compound, specifically the arrangement of atoms around the chiral center at the 4th position in a cis (same side) orientation.
6. Cyclic ether
4. A cyclic ether is a compound with an ether functional group (-O-) that forms a ring structure. In this case, the dioxolane ring is an example of a cyclic ether.
7. Flavoring agent in the food industry
5. This compound is used to add flavor to various food products due to its pleasant odor.
8. Used in fragrances and perfumes
6. The compound's pleasant odor also makes it suitable for use in the production of fragrances and perfumes.
9. Potential applications in pharmaceuticals
7. The compound may have potential uses in the development of pharmaceutical products, although specific applications are not mentioned.
10. Intermediate in organic synthesis
8. This compound can be used as a starting material or intermediate in the synthesis of other organic compounds.
11. Safety precautions
9. It is important to handle this chemical with care and follow safety guidelines when using it in laboratory or industrial settings to minimize potential hazards.
Check Digit Verification of cas no
The CAS Registry Mumber 124600-38-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,6,0 and 0 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 124600-38:
(8*1)+(7*2)+(6*4)+(5*6)+(4*0)+(3*0)+(2*3)+(1*8)=90
90 % 10 = 0
So 124600-38-0 is a valid CAS Registry Number.
124600-38-0Relevant articles and documents
METHOD FOR SYNTHESIZING SAPROPTERIN DIHYDROCHLORIDE
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Paragraph 0053, (2015/04/22)
Disclosed is a method for synthesizing sapropterin dihydrochloride. The present disclosure reduces a synthesis route of the sapropterin dihydrochloride, introduces a chiral center in an asymmetric synthesis manner, in which a tetrahydrofuran solution containing a samarium catalyst is adopted as a catalyst, and obtains a target compound having a high antimer isomerism value by means of selective catalysis. The yield is improved, raw materials are cheap and readily available, and the cost is significantly reduced, hence providing an effective scheme for mass industrial production of the sapropterin dihydrochloride.
METHOD FOR SYNTHESIZING SAPROPTERIN DIHYDROCHLORIDE
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, (2015/03/03)
Disclosed is a method for synthesizing sapropterin dihydrochloride. The present invention reduces a synthesis route of the sapropterin dihydrochloride, and resolves a racemate intermediate or an intermediate having a low antimer isomerism value by using a chiral resolving reagent, thereby obtaining an intermediate having a high antimer isomerism value. Raw materials are cheap and readily available, and the cost is significantly reduced, hence providing an effective scheme for mass industrial production of the sapropterin dihydrochloride.
ENZYMATIC ENANTIOSELECTIVE HYDROLYSIS OF 2,2-DIMETHYL-1,3-DIOXOLANE-4-CARBOXYLIC ESTERS
Pottie, M.,Eycken, J. Van der,Vandewalle, M.,Dewanckele, J. M.,Roeper, H.
, p. 5319 - 5322 (2007/10/02)
2,2-dimethyl-1,3-dioxolane-4-carboxylic acid derived chiral building blocks were prepared from substituted α,β-unsaturated acids with high enantiomeric purities by enzymatic hydrolysis of their n.butyl esters.
