148017-42-9 Usage
Molecular structure
The molecule contains a pyrrolidine ring, a carboxylic acid group, an acetylthio group, and a hydroxymethyl group.
Stereochemistry
The 2S,4S designation indicates the specific orientation of the two chiral centers in the molecule.
Boc-protected amino alcohol
It is a specific stereoisomer of a boc-protected amino alcohol, which is a compound used to protect amino alcohols during chemical reactions.
Use in organic synthesis and pharmaceutical research
The compound is used in organic synthesis and pharmaceutical research due to its unique structure and reactivity.
Potential applications in pharmaceuticals
The compound has potential applications in the development of pharmaceuticals and other biologically active compounds due to its unique structure and reactivity.
Check Digit Verification of cas no
The CAS Registry Mumber 148017-42-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,8,0,1 and 7 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 148017-42:
(8*1)+(7*4)+(6*8)+(5*0)+(4*1)+(3*7)+(2*4)+(1*2)=119
119 % 10 = 9
So 148017-42-9 is a valid CAS Registry Number.
InChI:InChI=1/C12H21NO4S/c1-8(15)18-10-5-9(7-14)13(6-10)11(16)17-12(2,3)4/h9-10,14H,5-7H2,1-4H3/t9-,10-/m0/s1
148017-42-9Relevant articles and documents
Synthesis and modification of a novel 1 β-methyl carbapenem antibiotic, S-4661
Iso,Irie,Iwaki,Kii,Sendo,Motokawa,Nishitani
, p. 478 - 484 (2007/10/03)
We describe an efficient method for introducing a sulfamoylamino group into the C-2' position of pyrrolidine using the Mitsunobu reaction. S-4661, its N-methyl analogues and stereoisomers were synthesized using this method and their structure-activity relationships were investigated.
