Welcome to LookChem.com Sign In|Join Free
  • or
(2R,1'R,5'R)-(-)-2-(2'-Azabicyclo[3.3.0]octan-2'-yl)-2-phenylethanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

180624-37-7

Post Buying Request

180624-37-7 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

180624-37-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 180624-37-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,0,6,2 and 4 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 180624-37:
(8*1)+(7*8)+(6*0)+(5*6)+(4*2)+(3*4)+(2*3)+(1*7)=127
127 % 10 = 7
So 180624-37-7 is a valid CAS Registry Number.

180624-37-7Relevant academic research and scientific papers

TRIAZOLOPYRIDINE COMPOUNDS

-

, (2012/12/14)

The present invention relates to the use of novel triazolopyridine derivatives of formula I: wherein all variable substituents are defined as described herein, which are SYK inhibitors and are useful for the treatment of auto-immune and inflammatory diseases.

TRIAZOLOPYRIDINE COMPOUNDS

-

, (2013/02/28)

The present invention relates to the use of novel triazolopyridine derivatives of formula I: wherein all variable substituents are defined as described herein, which are SYK inhibitors and are useful for the treatment of auto-immune and inflammatory diseases.

Utilization of industrial waste materials. Part 14.? Synthesis of -amino alcohols and thiols with a 2-azabicyclo[3.3.0]octane backbone and their application in enantioselective catalysis

Kossenjans, Michael,Soeberdt, Michael,Wallbaum, Sabine,Harms, Klaus,Martens, Juergen,Aurich, Hans Guenter

, p. 2353 - 2365 (2007/10/03)

New, chiral β-tert-amino tert-alcohols have been synthesized from the enantiomerically pure sec-amine (all-R)-lb via the new glycine, alanine and phenylglycine derivatives 2-6. Grignard additions to these esters provided the new rigid amino alcohols 7-11 in fair yields. The absolute configurations of the stereogenic centers, which arose during the alkylation step, were assigned by an independent route leading to some of the optical antipodes of 7-10. Condensation of enantiomerically pure β-amino alcohols 13a-g, 16 and 17 with y-ketoester rac-12 afforded the TV; O-acetals 14a-g, 18 and 19, which were subsequently reduced to the β-/e/7-amino alcohols 10a,c and 15a-g. X-Ray analysis of compound 19 was performed to verify the stereochemistry observed by chemical correlation. The nucleophilic ring opening of enantiomerically pure styrene oxide by amine Ib resulted in the formation of regioisomeric amino alcohols 9a, 21a, and lOa, 21b. Amino thiol derivatives 22 and 25a,b were prepared by treatment of 10a-and 15a,b, respectively, with methanesulfonyl chloride followed by regio- and stereoselective cleavage of the situ formed aziridinium ions with potassium thioacetate. Reduction of these compounds to thiols 23 and 26a,b and subsequent oxidation afforded amino disulfides 24 and 27a,b. Finally, the bicyclic β-amino alcohols and thiols were used as chiral ligands in the enantioselective addition of diethylzinc to benzaldehyde and ee values up to 96% were found. ;.

Functionalized 2-azabicyclo[3.3.0]octanes as ligands in the enantioselective catalysis

Aurich, Hans Guenter,Soeberdt, Michael

, p. 2553 - 2554 (2007/10/03)

Enantiopure compounds 4 were prepared by condensation of β- aminoalcohols 2 with ethyl (2-oxocyclopentyl)acetate 1 and subsequent reduction of intermediates 3. Compound 4a was converted to 6 via 5. With compounds 4, 5 or 6 as chiral ligands in the reaction of benzaldehyde with diethylzine an enantiomeric excess between 14 and 84% was achieved.

Asymmetric synthesis of cis-fused bicyclic pyrrolidines and pyrrolidinones via chiral polycyclic lactams

Ennis, Michael D.,Hoffman, Robert L.,Ghazal, Nabil B.,Old, David W.,Mooney, Pamela A.

, p. 5813 - 5817 (2007/10/03)

Condensation of racemic keto-ester 2 and 1.1 equiv of (R)-(-)-phenylglycinol in toluene with azeotropic removal of water and methanol gave rise to a tetracyclic lactam in greater than 90% yield. Examination of the crude reaction product by 1H and 13C NMR, capillary GC, and HPLC revealed this product to be a single isomer, the absolute configuration of which was determined to be that illustrated by structure 3. The tetracyclic lactam 3 was stereospecifically reduced to either the cis-fused bicyclic pyrrolidine 4 or the cis-fused bicyclic pyrrolidinone 9. The chiral auxiliaries in both 4 and 9 were removed using different, novel methodologies. This highly stereoselective reaction establishes two contiguous chiral centers via the deracemization of an achiral keto-ester. This methodology has been applied to the synthesis of (1R,5R)-2-azabicyclo[3.3.0]octane 15. This important amine is now readily available from commercial materials in only three steps.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 180624-37-7
  • ©2008 LookChem.com,License:ICP NO.:Zhejiang16009103 complaints:service@lookchem.com
  • [Hangzhou]86-0571-87562588,87562578,87562573 Our Legal adviser: Lawyer