1143534-07-9Relevant articles and documents
Catalytic asymmetric mannich reactions of sulfonylacetates
Cassani, Carlo,Bernardi, Luca,Fini, Francesco,Ricci, Alfredo
supporting information; experimental part, p. 5694 - 5697 (2009/11/30)
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1143534-07-9
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Basic information
- Product Name: (S)-methyl 3-(tert-butoxycarbonyl)-3-(4-chlorophenyl)propanoate
- Synonyms: (S)-methyl 3-(tert-butoxycarbonyl)-3-(4-chlorophenyl)propanoate
- CAS NO:1143534-07-9
- Molecular Formula:
- Molecular Weight: 313.781
- EINECS: N/A
- Product Categories: N/A
- Mol File: 1143534-07-9.mol
- Article Data: 2
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Chemical Properties
- Melting Point: N/A
- Boiling Point: 426.2±40.0 °C(Predicted)
- Flash Point: N/A
- Appearance: N/A
- Density: 1.178±0.06 g/cm3(Predicted)
- Refractive Index: N/A
- Storage Temp.: N/A
- Solubility: N/A
- CAS DataBase Reference: (S)-methyl 3-(tert-butoxycarbonyl)-3-(4-chlorophenyl)propanoate(CAS DataBase Reference)
- NIST Chemistry Reference: (S)-methyl 3-(tert-butoxycarbonyl)-3-(4-chlorophenyl)propanoate(1143534-07-9)
- EPA Substance Registry System: (S)-methyl 3-(tert-butoxycarbonyl)-3-(4-chlorophenyl)propanoate(1143534-07-9)
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Safety Data
- Hazard Codes: N/A
- Statements: N/A
- Safety Statements: N/A
- WGK Germany:
- RTECS:
- HazardClass: N/A
- PackingGroup: N/A
- Hazardous Substances Data: 1143534-07-9(Hazardous Substances Data)
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1143534-07-9 Usage
Description
(S)-methyl 3-(tert-butoxycarbonyl)-3-(4-chlorophenyl)propanoate, with the molecular formula C17H21ClO4, is a chiral ester compound that serves as a crucial intermediate in the synthesis of pharmaceuticals and agrochemicals. As a derivative of (S)-ibuprofen, a well-known nonsteroidal anti-inflammatory drug, it plays a significant role in the development of various medications aimed at treating pain and inflammation.Uses
Used in Pharmaceutical Industry:(S)-methyl 3-(tert-butoxycarbonyl)-3-(4-chlorophenyl)propanoate is used as an intermediate in the synthesis of various drugs for the treatment of pain and inflammation. Its role in the production of medications is due to its structural similarity to (S)-ibuprofen, which allows for the development of new drug compounds with potentially improved efficacy and reduced side effects.
Used in Research and Development:
(S)-methyl 3-(tert-butoxycarbonyl)-3-(4-chlorophenyl)propanoate is also utilized in the research and development of novel drug compounds. Its unique structure and properties make it a valuable tool for scientists and researchers in the pharmaceutical industry, as they explore new avenues for drug discovery and innovation.
Used in Agrochemical Industry:
In addition to its applications in the pharmaceutical sector, (S)-methyl 3-(tert-butoxycarbonyl)-3-(4-chlorophenyl)propanoate is also used as an intermediate in the synthesis of agrochemicals. Its role in this industry is attributed to its ability to contribute to the development of new compounds with potential applications in agriculture, such as pesticides or herbicides.
Used in Chiral Auxiliaries and Advanced Materials:
Furthermore, (S)-methyl 3-(tert-butoxycarbonyl)-3-(4-chlorophenyl)propanoate is a key ingredient in the production of chiral auxiliaries and advanced materials in the pharmaceutical industry. Chiral auxiliaries are essential in the synthesis of enantiomerically pure compounds, which are crucial for the development of drugs with specific therapeutic effects. (S)-methyl 3-(tert-butoxycarbonyl)-3-(4-chlorophenyl)propanoate's role in this area highlights its versatility and importance in the field of pharmaceutical chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 1143534-07-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,4,3,5,3 and 4 respectively; the second part has 2 digits, 0 and 7 respectively.Calculate Digit Verification of CAS Registry Number 1143534-07:
(9*1)+(8*1)+(7*4)+(6*3)+(5*5)+(4*3)+(3*4)+(2*0)+(1*7)=119
119 % 10 = 9
So 1143534-07-9 is a valid CAS Registry Number.
1143534-07-9Upstream product
1143534-07-9Downstream Products
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(S)-methyl 3-(tert-butoxycarbonyl)-3-(4-chlorophenyl)propanoate
