51077-13-5 Usage
General Description
1-(tert-butoxycarbonyl)-2,5-dihydro-1H-pyrrole-2-carboxylic acid, also known as Boc-D-pyrrole-2-carboxylic acid, is a chemical compound commonly used in organic synthesis for the protection and deprotection of amines. It is a derivative of pyrrole and belongs to the class of pyrrole-2-carboxylic acids. With a tert-butoxycarbonyl (Boc) protecting group, it serves as a versatile building block for the synthesis of various complex molecules and pharmaceuticals. It is used in the pharmaceutical industry for the development and production of drugs, including antiviral and antibacterial agents. Additionally, it has applications in the field of medicinal chemistry and drug discovery.
Check Digit Verification of cas no
The CAS Registry Mumber 51077-13-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,0,7 and 7 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 51077-13:
(7*5)+(6*1)+(5*0)+(4*7)+(3*7)+(2*1)+(1*3)=95
95 % 10 = 5
So 51077-13-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H15NO4/c1-10(2,3)15-9(14)11-6-4-5-7(11)8(12)13/h4-5,7H,6H2,1-3H3,(H,12,13)
51077-13-5Relevant articles and documents
NOVEL HETEROCYCLIC AMIDE DERIVATIVES HAVING DIHYDROOROTATE DEHYDROGENASE INHIBITING ACTIVITY
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Page/Page column 66, (2010/10/20)
Novel heterocyclic amide derivatives having pharmacological effects, that is, compounds represented by the general formula (1) or salts thereof: (1) wherein X1-X2 is S-CH2 or the like; R1 is alkyl or the like; p is 0 to 7; R2 is hydrogen, alkyl, or the like; R3 is hydrogen, alkyl, or the like; Y1-Y2 is CH=CH or the like; R4 is halogeno, alkyl, or the like; q is 0 to 4; and R5 is halogeno, hydrogen, alkyl, or the like.
Synthesis of Two Naturally Occuring Diastereomeric Dihydroxyprolines: 2,3-trans-3,4-trans-3,4-Dihydroxy-L-proline and 2,3-cis-3,4-trans-3,4-Dihydroxy-L-proline
Kahl, Jens-Uwe,Wieland, Theodor
, p. 1445 - 1450 (2007/10/02)
Starting from 2-pyrrolecarboxylic acid the N-Boc derivative 6 is resolved into its optically active constituents by crystalisation with R(+)-1-(4-nitrophenyl)ethaneamin.The N-tosyl-3,4-dehydro-L-proline methyl ester (L-7) derived from this is converted by
