120851-71-0 Usage
Uses
Used in Pharmaceutical Industry:
Trans-1-Benzoyl-4-phenyl-L-proline is used as a key intermediate in the synthesis of drugs, particularly angiotensin-converting enzyme (ACE) inhibitors. These ACE inhibitors are crucial in the treatment of high blood pressure and heart failure, as they help regulate blood pressure and improve heart function.
Used in Drug Synthesis:
Trans-1-Benzoyl-4-phenyl-L-proline is used as a building block in the development of new pharmaceutical compounds. Its unique structure, which includes a benzoyl group, a phenyl group, and a proline residue, allows for the creation of various drug molecules with potential therapeutic applications. This makes it a valuable component in the field of medicinal chemistry and drug discovery.
Check Digit Verification of cas no
The CAS Registry Mumber 120851-71-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,8,5 and 1 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 120851-71:
(8*1)+(7*2)+(6*0)+(5*8)+(4*5)+(3*1)+(2*7)+(1*1)=100
100 % 10 = 0
So 120851-71-0 is a valid CAS Registry Number.
InChI:InChI=1/C18H17NO3/c20-17(14-9-5-2-6-10-14)19-12-15(11-16(19)18(21)22)13-7-3-1-4-8-13/h1-10,15-16H,11-12H2,(H,21,22)/t15?,16-/m0/s1
120851-71-0Relevant articles and documents
Preparation methods of antihypertensive Fosinopril sodium and key intermediate thereof
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Paragraph 0014, (2017/12/14)
The invention relates to preparation methods of an antihypertensive Fosinopril sodium and a key intermediate thereof trans-4-phenyl-L-proline suitable for industrial production. Synthesis of the key intermediate trans-4-phenyl-L-proline has high chiral selectivity, and the method is simple and easy to operate.
Stereospecific Friedel-Crafts alkylation of benzene with 4-mesyloxy-L-prolines. A new synthesis of 4-phenylprolines
Kronenthal,Mueller,Kuester,Kissick,Johnson
, p. 1241 - 1244 (2007/10/02)
The reaction of benzene with cis- and trans-N-benzoyl-4-mesyloxy-L-proline (11 and 12) in the presence of AlCl3 stereospecifically produces the corresponding trans- and cis-4-phenylproline derivatives.