173154-00-2 Usage
General Description
The chemical compound "(S)-4-Benzyl-3-((S)2-((R) -2-BroMo-2((2S,4S)-4-isopropyl-5-oxo-tetrahydro-furan-2-yl)-3-Methyl-butyryl)-oxaxolidin-2-one" is a complex molecule composed of various functional groups. It consists of a benzyl group, a bromo-substituted oxazolidinone ring, and a tetrahydrofuran ring with an isopropyl and methyl-butyryl substituent. The compound has multiple chiral centers, indicated by the (S) and (R) prefixes, resulting in a stereochemically complex structure. (S)-4-Benzyl-3-((S)2-((R) -2-BroMo-2((2S,4S)-4-isopropyl-5-
oxo-tetrahydro-furan-2-yl)-3-Methyl-butyryl)-oxaxolidin-2-one likely has diverse applications in organic chemistry, pharmaceuticals, and material science due to its intricate structure and potential reactivity.
Check Digit Verification of cas no
The CAS Registry Mumber 173154-00-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,3,1,5 and 4 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 173154-00:
(8*1)+(7*7)+(6*3)+(5*1)+(4*5)+(3*4)+(2*0)+(1*0)=112
112 % 10 = 2
So 173154-00-2 is a valid CAS Registry Number.
InChI:InChI=1/C24H32BrNO5/c1-14(2)18(11-20(25)21-12-19(15(3)4)23(28)31-21)22(27)26-17(13-30-24(26)29)10-16-8-6-5-7-9-16/h5-9,14-15,17-21H,10-13H2,1-4H3/t17-,18-,19-,20+,21-/m0/s1
173154-00-2Relevant articles and documents
A Facile, Six-Step Process for the Synthesis of (3 S,5 S)-3-Isopropyl-5-((2 S,4 S)-4-isopropyl-5-oxo-tetrahydrofuran-2-yl)-2-oxopyrrolidine-1-carboxylic Acid tert -Butyl Ester, the Key Synthetic Intermediate of Aliskiren
Pan, Xianhua,Xu, Siyao,Huang, Rui,Yu, Wansheng,Liu, Feng
, p. 611 - 617 (2015/06/30)
A facile, six-step process for the synthesis of (3S,5S)-3-isopropyl-5-((2S,4S)-4-isopropyl-5-oxotetrahydro- furan-2-yl)-2-oxopyrrolidine-1-carboxylic acid tert-butyl ester from (S)-4-benzyloxazolidin-2-one 2 in an overall 50% yield is reported. The key transformations include: a highly efficient diastereoselective epoxidation, Lewis acid-catalyzed ring-opening with bromide, an SN2 reaction using NaN3, and a tandem reduction-cyclization reaction.
DELTA-AMINO-GAMMA-HYDROXY-OMEGA-ARYL-ALKANOIC ACID AMIDES
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, (2008/06/13)
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