1143534-42-2Relevant 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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1143534-42-2
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Basic information
- Product Name: (R)-methyl 3-(tert-butoxycarbonyl)-3-(4-chlorophenyl)propanoate
- Synonyms: (R)-methyl 3-(tert-butoxycarbonyl)-3-(4-chlorophenyl)propanoate
- CAS NO:1143534-42-2
- Molecular Formula:
- Molecular Weight: 313.781
- EINECS: N/A
- Product Categories: N/A
- Mol File: 1143534-42-2.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: (R)-methyl 3-(tert-butoxycarbonyl)-3-(4-chlorophenyl)propanoate(CAS DataBase Reference)
- NIST Chemistry Reference: (R)-methyl 3-(tert-butoxycarbonyl)-3-(4-chlorophenyl)propanoate(1143534-42-2)
- EPA Substance Registry System: (R)-methyl 3-(tert-butoxycarbonyl)-3-(4-chlorophenyl)propanoate(1143534-42-2)
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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: 1143534-42-2(Hazardous Substances Data)
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1143534-42-2 Usage
Description
(R)-methyl 3-(tert-butoxycarbonyl)-3-(4-chlorophenyl)propanoate is a chemical compound with a molecular formula of C17H21ClO4. It is a derivative of the amino acid proline and is characterized by its unique structure, which includes a tert-butoxycarbonyl (Boc) protecting group. (R)-methyl 3-(tert-butoxycarbonyl)-3-(4-chlorophenyl)propanoate is known for its role as a building block in organic synthesis, particularly in the creation of pharmaceutical drugs and other biologically active compounds.Uses
Used in Pharmaceutical Industry:(R)-methyl 3-(tert-butoxycarbonyl)-3-(4-chlorophenyl)propanoate is used as a building block for the synthesis of various pharmaceutical drugs. Its role in this industry is crucial due to its ability to contribute to the development of new medications that can address a wide range of health conditions.
Used as a Chiral Building Block:
In the synthesis of chiral pharmaceuticals, agrochemicals, and biologically active compounds, (R)-methyl 3-(tert-butoxycarbonyl)-3-(4-chlorophenyl)propanoate serves as a valuable chiral building block. The importance of chirality in these applications is significant, as it can influence the effectiveness and safety of the final product.
Used in Organic Synthesis:
(R)-methyl 3-(tert-butoxycarbonyl)-3-(4-chlorophenyl)propanoate is also widely utilized as a versatile intermediate in the production of various pharmaceutical compounds. The presence of the Boc protecting group allows for the selective protection of the amine group during organic synthesis, which is essential for the successful synthesis of complex molecular structures.
Check Digit Verification of cas no
The CAS Registry Mumber 1143534-42-2 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, 4 and 2 respectively.Calculate Digit Verification of CAS Registry Number 1143534-42:
(9*1)+(8*1)+(7*4)+(6*3)+(5*5)+(4*3)+(3*4)+(2*4)+(1*2)=122
122 % 10 = 2
So 1143534-42-2 is a valid CAS Registry Number.
1143534-42-2Upstream product
1143534-42-2Downstream Products
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(R)-methyl 3-(tert-butoxycarbonyl)-3-(4-chlorophenyl)propanoate
